urn:gs1:gdd:cl:AdditionalTradeItemIdentificationTypeCode Additional trade item identification type Typ av kompletterande artikelidentitet 11 2026-08-22 gdsn ADMDM false Agence du Médicament de Madagascar Agency du Médicament de Madagascar manages the market authorisation of healthcare products in Madagascar - MG AE_MOHAP false UAE Ministry of Health and Prevention (MOHAP) Ministry of Health and Prevention (MOHAP) manages the market authorisation of healthcare products in United Arab Emirates - AE. AIG false Active Ingredient Number The Active Ingredient Group Number specifies the a number assigned by Health Canada in the Drug Product Database. The AIG number is a 10 digit number that identifies products that have the same active ingredient(s) and ingredient strength(s). ANATEL false ANATEL Brazil's Federal Telecommunications Agency ANDA false FDA Abbreviated New Drug Application (ANDA) Number An abbreviated new drug application (ANDA) contains data which is submitted to FDA for the review and potential approval of a generic drug product. https://www.fda.gov/drugs/types-applications/abbreviated-new-drug-application-anda ANVISA false Brazil National Health Surveillance Agency (ANVISA) National Health Surveillance Agency (ANVISA) manages the market authorisation of healthcare products in Brazil - BR AO_DNME false Angola Direcção Nacional de Medicamentos e Equipamentos (DNME) Direcção Nacional de Medicamentos e Equipamentos (DNME) manages the market authorisation of healthcare products in Angola - AO. ARFA false Agência de Regulação e Supervisão dos Produtos Farmacêuticos e Alimentares (ARFA) Agência de Regulação e Supervisão dos Produtos Farmacêuticos e Alimentares (ARFA) manages the market authorisation of healthcare products in Cape Verde - CV ARTG_ID false Australian Register of Therapeutic Goods The Australian Therapeutic Goods Administration (TGA) is a government organisation responsible for the regulation of therapeutic goods such as medicines and medical devices. Once a product is accepted for sale in Australia (via TGA approval) this item is listed on the Australian Register of Therapeutic Goods (ARTG). All goods within Australia, or to be exported from Australia, must be present on this list before they can be available. Information held in the database includes the name of the product, what it contains and manufacturer details. AU_PROSTHESES_REBATE_CODE false Australian Prostheses Rebate Code In Australia the federal government, through the Department of Health and Ageing, provide a rebate to private health hospitals or clinics to cover the cost of any prostheses that are fitted to a patient. This rebate is designed to cover the costs incurred by the provider. Every product is given a ‘billing code’ from the Department of Health and Ageing. This is used by the provider to communicate the rebate request to the government. BB_DS false Barbados Drug Service (DS) Barbados Drug Service (DS) manages the market authorisation of healthcare products in Barbados - BB. BE_FAMHP false Belgium Federal Agency for Medicines and Health Products (FAMHP) : CNK Number Belgiska federala läkemedels- och hälsomyndigheten (FAMHP): CNK-nummer Federal Agency for Medicines and Health Products (FAMHP) manages the market authorisation of healthcare products in Belgium - BE with a National Code Number (CNK). The CNK code attributed by the APB. (Association Pharma Belgium) Cannot be edited afterhand in alignment with the CNK allocation rules (No edit, no change, no deletion. BE_FAMHP_NN false Belgium Federal Agency for Medicines and Health Products (FAMHP) : Notification number Belgiska federala läkemedels- och hälsomyndigheten (FAMHP): Anmälningsnummer The notification number for implants and long-term invasive medical devices is mandatory. https://www.vas.ehealth.fgov.be/registers/sadm/web/search/public. Anmälningsnumret för implantat och långvariga invasiva medicintekniska produkter är obligatoriskt. https://www.vas.ehealth.fgov.be/registers/sadm/web/search/public. BFR false Number of the German Federal Institute for Risk Assessment (BFR) - Germany The Federal Institute for Risk Assessment (BFR - Bundesinstitut für Risikobewertung) in the field of consumer health protection. The BFR number is a so-called product identification element (PI element). The PI element consists of the five-digit BFR company code and a four-digit number allocated by the manufacturer itself. The number sequence ends with details of the hazard characteristics of the product (for instance, irritant, corrosive or toxic). BG_BDA false Bulgarian Drug Agency (BDA) Bulgarian Drug Agency (BDA) manages the market authorisation of healthcare products in Bulgaria - BG. BI_ABREMA false Burundi l’Autorité Burundaise de Régulation des Médicaments et des Aliments (ABREMA) l’Autorité Burundaise de Régulation des Médicaments et des Aliments (ABREMA) manages the market authorisation of healthcare products in Burundi - BI. BJ_DPMED false Benin Direction de la Pharmacie, du Medicament et des Explorations Diagnostiques (DPMED) Direction de la Pharmacie, du Medicament et des Explorations Diagnostiques (DPMED) manages the market authorisation of healthcare products in Benin - BJ. BNDA false Bahamas National Drug Agency (BNDA) Bahamas National Drug Agency (BNDA) manages the market authorisation of healthcare products in Bahamas - BS BUYER_ASSIGNED Buyer Assigned Köparens artikelnummer A proprietary internal identification number assigned by a data recipient, used to identify trade items purchased from each trading partner with whom they engage in a commercial relationship. Artikelnummer som tilldelas av köparen. BUYER_ASSIGNED_USED_BY_THIRD_PARTY false Buyer Assigned used by Third Party The proprietary number that is assigned by a third party buyer whose number is required by the data recipient in the trading relationship, that is used to identify trade items purchased from the supplier in addition to the GTIN. Example Identification number assigned by the buyer for use by a marketplace. BW_BOMRA false Botswana Medicines Regulatory Authority (BoMRA) Botswana Medicines Regulatory Authority (BoMRA) manages the market authorisation of healthcare products in Botswana - BW. CDSCO false India Central Drugs Standard Control Organization (CDSCO) Central Drugs Standard Control Organization (CDSCO) manages the market authorisation of healthcare products in India - IN CL_ISP false Chile Instituto de Salud Pública (ISP) Instituto de Salud Pública (ISP) manages the market authorisation of healthcare products in Chile - CL. CM_LANACOME false Cameroon Laboratoire National de Contrôle de Qualité des Médicaments et d’Expertise (LANACOME) Laboratoire National de Contrôle de Qualité des Médicaments et d’Expertise (LANACOME) ensure the quality control of drugs and other health products in Cameroon - CM. CPNP false Cosmetic Products Notification Portal (CPNP) reference The Cosmetic Products Notification Portal (CPNP) is an online database created by the European Union for the implementation of Regulation (EC) No 1223/2009, in which cosmetics are registered and documented. Each product is assigned a unique CPNP reference when it is registered. CZ_SUKL false SUKL code (Czech Republic) The SÚKL code is a unique identifier used by the State Institute for Drug Control (SÚKL) in the Czech Republic. It uniquely identifies a specific medicinal product or medical device in the SÚKL database. DAV false Vietnam Drug Administration of Vietnam (DAV) Drug Administration of Vietnam (DAV) manages the market authorisation of healthcare products in Viet Nam - VN DDA_NP false Nepal Department of Drug Administration (DDA) Department of Drug Administration (DDA) manages the market authorisation of healthcare products in Nepal - NP DDF_KH false Cambodia Department of Drugs and Food (DDF) Department of Drugs and Food (DDF) manages the market authorisation of healthcare products in Cambodia - KH DDSME false Kyrgyzstan Department of Drug Supply and Medical Equipment Department of Drug Supply and Medical Equipment manages the market authorisation of healthcare products in Kyrgyzstan - KG DE_BFARM false Germany Federal Institute for Drugs and Medical Devices (BfArM) Federal Institute for Drugs and Medical Devices (BfArM) manages the market authorisation of healthcare products in Germany - DE. DGDA false Bangladesh Directorate General of Drug Administration (DGDA) Directorate General of Drug Administration (DGDA) manages the market authorisation of healthcare products in Bangladesh - BD DGPML_BF false Burkina Faso Direction Générale de la Pharmacie, du Médicament et des Laboratoires (DGPML) Direction Générale de la Pharmacie, du Médicament et des Laboratoires (DGPML) manages the market authorisation of healthcare products in Burkina Faso - BF DGPML_BJ false Benin Direction General of Pharmacy, Medicine and Pharmacy Laboratories (DGPML) Direction General of Pharmacy, Medicine and Pharmacy Laboratories (DGPML) manages the market authorisation of healthcare products in Benin - BJ DGRS false Honduras Direccion General de Regulacion Sanitaria (DGRS) Direccion General de Regulacion Sanitaria (DGRS) manages the market authorisation of healthcare products in Honduras - HN DIGEMID_MINSA false Peru Dirección General de Medicamentos (DIGEMID-MINSA) Dirección General de Medicamentos (DIGEMID-MINSA) manages the market authorisation of healthcare products in Peru - PE DIN false Drug Identification Number (DIN) - Canada A Drug Identification Number (DIN) is a computer-generated eight digit number assigned by Health Canada to a drug product prior to being marketed in Canada. DIN_HM false Drug Identification Number - Homeopathic Medicine (DIN HM) - Canada Drug Identification Number – Homeopathic Medicine: This is the number located on the label of homeopathic drug products that have been approved for sale in Canada. DISTRIBUTOR_ASSIGNED not defined Distributörens artikelnummer The additional Trade Item Identification value populated has been developed and assigned by an entity which purchases and takes title to goods which are then resold / redistributed elsewhere. Artikelnummer som tilldelas av distributören. DLP false Direction des Laboratoires et des Pharmacies Direction des Laboratoires et des Pharmacies manages the market authorisation of healthcare products in Comoros - KM DNM_SV false El Salvador Dirección Nacional de Medicamentos (DNM) Dirección Nacional de Medicamentos (DNM) manages the market authorisation of healthcare products in El Salvador - SV DNPL false Guinea Direction Nationale de la Pharmacie et du Laboratoire Direction Nationale de la Pharmacie et du Laboratoire manages the market authorisation of healthcare products in Guinea - GN DPL false Senegal Direction de la Pharmacie et des Laboratoires Direction de la Pharmacie et des Laboratoires manages the market authorisation of healthcare products in Senegal - SN DPLMT false Direction des Dervices Pharmaceutiques des Laboratoires et de la Médecine Traditionnelle Direction des services Pharmaceutiques des laboratoires et de la Médecine Traditionnelle manages the market authorisation of healthcare products in Central African Republic - CF DPML false Cote d'Ivoire Direction de la Pharmacie, du Médicament et des Laboratoires (DPML) Direction de la Pharmacie, du Médicament et des Laboratoires (DPML) manages the market authorisation of healthcare products in Cameroon - CM DPMLMOH false Burundi Department of Pharmacy, Medicines and Laboratory, Ministry of Health Department of Pharmacy, Medicines and Laboratory, Ministry of Health manages the market authorisation of healthcare products in Burundi - BI DPM_CD false Democratic Republic of Congo Direction de la Pharmacie et du Médicament DPM Direction de la Pharmacie et du Médicament (DPM) manages the market authorisation of healthcare products in Congo, Democratic Republic of - CD DPM_CI false Direction de la Pharmacie et du Médicament DPM Côte d'Ivoire Direction de la Pharmacie et du Médicament (DPM) manages the market authorisation of healthcare products in Côte d'Ivoire - CI DPM_ML false Mali Direction de la Pharmacie et du Médicament Direction de la Pharmacie et du Médicament manages the market authorisation of healthcare products in Mali - ML DRAP false Drug Regulatory Authority of Pakistan (DRAP) Drug Regulatory Authority of Pakistan (DRAP) manages the market authorisation of healthcare products in Pakistan - PK DRA_BT false Drug Regulatory Authority (DRA) Drug Regulatory Authority (DRA) manages the market authorisation of healthcare products in Bhutan - BT DTAMOH false Directorate of Technical Affairs in the Ministry of Health Directorate of Technical Affairs in the Ministry of Health manages the market authorisation of healthcare products in Iraq - IQ EC_ANRCVS false Ecuador Agencia Nacional de Regulación, Control, y Vigilancia Sanitaria (ANRCVS) Agencia Nacional de Regulación, Control, y Vigilancia Sanitaria (ANRCVS) manages the market authorisation of healthcare products in Ecuador - EC. EDA false Egyptian Drug Authority (EDA) Egyptian Drug Authority (EDA) manages the market authorisation of healthcare products in Egypt - EG EPD false EPD Electronisk Produkt Database Identifier: EPREL EPREL Registration Number EPREL-registreringsnummer Model registration number assigned by EPREL (European Product Registry for Energy Labelling) when the product record is created in this database. It can be used to access public information about the product in EPREL, e.g., its energy label. EPREL-registreringsnummer som tilldelas av EPREL (European Product Registry for Energy Labelling). ET_EFDA false Ethiopian Food and Drug Administration (EFDA) Ethiopian Food and Drug Administration (EFDA) manages the market authorisation of healthcare products in Ethiopia - ET. EUDAMED false EUDAMED Device Identifier EUDAMED Device Identifier EU_MEDICAL_PRODUCT_NUMBER false EU medicinal product number The European Commission for Public Health has procedures for centrally authorised medicinal products, and holds community registers for: - medicinal products for human use (regulation (EC) 726/2004) - orphan medicinal products for human use (regulation (EC) N141/2000) - veterinary medicinal products (regulation (EE) 726/2004). FDA_MEDICAL_DEVICE_LISTING false FDA Medical Device Listing Most Owners or operators of places of business (also called establishments or facilities) that are involved in the production and distribution of medical devices intended for use in the United States (U.S.) are required to list the devices that are made at their facility and the activities that are performed on those devices. Registration and listing provides FDA with the location of medical device establishments and the devices manufactured at those establishments. Knowing where devices are made increases the nation’s ability to prepare for and respond to public health emergencies. FDA_MM false Food and Drug Administration (FDA) Myanmar Food and Drug Administration (FDA) manages the market authorisation of healthcare products in Myanmar - MM FDA_NDC_10 false FDA NDC 10 The National Drug Code of the United States of America is a unique 10-digit, 3-segment number assigned to each medication listed under Section 510 of the U.S. Federal Food, Drug, and Cosmetic Act. The number identifies the labeller or vendor, product, and trade package size. FDA_NDC_11 false not defined The National Drug Code of the United States of America is a unique 11-digit, 3-segment number assigned to each medication listed under Section 510 of the U.S. Federal Food, Drug, and Cosmetic Act. The number identifies the labeller or vendor, product, and trade package size. FDA_PH false Food and Drug Administration (FDA) Philippines Food and Drug Administration (FDA) manages the market authorisation of healthcare products in Philippines - PH FDA_PRODUCT_CODE false FDA Product Code The FDA Product Code describes a product or a group of products. It is a seven-character alphanumeric string composed of five components, the Product Industry Code, the Class Code, the Subclass Code, the Process Indicator Code, and the Group Code. For more in-depth information about the FDA Product Code, see Lessons 1, 3 and 4 of the FDA Office of Regulatory Affairs (ORA) Product Code Builder Tutorial (http://www.accessdata.fda.gov/scripts/ora/pcb/tutorial/tutorial.cfm). FDA_TH false Thai Food and Drug Administration (Thai FDA) Thai Food and Drug Administration (Thai FDA) manages the market authorisation of healthcare products in Thailand - TH FDB false Ghana Food and Drugs Board (FDB) Food and Drugs Board (FDB) manages the market authorisation of healthcare products in Ghana - GH FDD false Lao Food and Drug Department Food and Drug Department manages the market authorisation of healthcare products in Lao People’s Democratic Republic - LA FMHACA_ET false Food, Medicine and Health Care Administration and Control of Ethiopia (FMHACA) Food, Medicine and Health Care Administration and Control of Ethiopia (FMHACA) manages the market authorisation of healthcare products in Ethiopia - ET FOR_INTERNAL_USE_1 false For internal use 1 Identification used for internal mapping purposes. FOR_INTERNAL_USE_10 false For internal use 10 Identification used for internal mapping purposes. FOR_INTERNAL_USE_11 false For internal use 11 Identification used for internal mapping purposes. FOR_INTERNAL_USE_12 false For internal use 12 Identification used for internal mapping purposes. FOR_INTERNAL_USE_13 false For internal use 13 Identification used for internal mapping purposes. FOR_INTERNAL_USE_14 false For internal use 14 Identification used for internal mapping purposes. FOR_INTERNAL_USE_15 false For internal use 15 Identification used for internal mapping purposes. FOR_INTERNAL_USE_16 false For internal use 16 Identification used for internal mapping purposes. FOR_INTERNAL_USE_17 false For internal use 17 Identification used for internal mapping purposes. FOR_INTERNAL_USE_18 false For internal use 18 Identification used for internal mapping purposes. FOR_INTERNAL_USE_19 false For internal use 19 Identification used for internal mapping purposes. FOR_INTERNAL_USE_2 false For internal use 2 Identification used for internal mapping purposes. FOR_INTERNAL_USE_20 false For internal use 20 Identification used for internal mapping purposes. FOR_INTERNAL_USE_3 false For internal use 3 Identification used for internal mapping purposes. FOR_INTERNAL_USE_4 false For internal use 4 Identification used for internal mapping purposes. FOR_INTERNAL_USE_5 false For internal use 5 Identification used for internal mapping purposes. FOR_INTERNAL_USE_6 false For internal use 6 Identification used for internal mapping purposes. FOR_INTERNAL_USE_7 false For internal use 7 Identification used for internal mapping purposes. FOR_INTERNAL_USE_8 false For internal use 8 Internal identification used for mapping purposes. FOR_INTERNAL_USE_9 false For internal use 9 Internal identification used for mapping purposes. GA_DMP false Gabon Direction Médicament et de la Pharmacie Direction Médicament et de la Pharmacie (DMP) manages the market authorisation of healthcare products in Gabon- GA GA_MS false Gabon Ministry of Health Ministère de la Santé (MS) - Ministry of Health - manages the market authorisation of healthcare products in Gabon - GA. GDPA false Afghanistan General Directorate of Pharmaceutical Affairs (GDPA) General Directorate of Pharmaceutical Affairs (GDPA) manages the market authorisation of healthcare products in Afghanistan - AF GH_FDA false Ghana Food and Drugs Authority (FDA) Food and Drugs Authority (FDA) manages the market authorisation of healthcare products in Ghana - GH. GN_DNPM false US General Services Administration Special Item Number (SIN) A U.S. General Services Administration (GSA) Special Item Number (SIN) is a five-digit code that identifies and categorizes specific products and services offered under a GSA Schedule contract, making it easier for federal agencies to find and purchase the items they need. GSA_SIN false US General Services Administration Special Item Number (SIN) A U.S. General Services Administration (GSA) Special Item Number (SIN) is a five-digit code that identifies and categorizes specific products and services offered under a GSA Schedule contract, making it easier for federal agencies to find and purchase the items they need. GTIN_12 false GTIN 12 The 12-digit GS1 Identification Key composed of a U.P.C. Company Prefix, Item Reference, and Check Digit used to identify trade items. GTIN_13 false GTIN 13 The 13-digit GS1 Identification Key composed of a GS1 Company Prefix, Item Reference, and Check Digit used to identify trade items. GTIN_14 false GTIN 14 The 14-digit GS1 Identification Key composed of an Indicator digit (1-9), GS1 Company Prefix, Item Reference, and Check Digit used to identify trade items. GTIN_8 false GTIN 8 The 8-digit GS1 Identification Key composed of a GS1-8 Prefix, Item Reference, and Check Digit used to identify trade items. GY_GA-FDD false Guyana Government Analyst - Food and Drug Department (GA-FDD) Government Analyst - Food and Drug Department (GA-FDD) manages the market authorisation of healthcare products in Guyana - GY. HIBC false HIBC Health Industry Business Communication Barcode: An alphanumeric identification number used as a common identifier within the healthcare industry across different locations. In the Netherlands, this code is managed by the European Health Industry Business Communications Council. HN_ARSA false Honduras Agencia de Regulación Sanitaria (ARSA) Agencia de Regulación Sanitaria (ARSA) manages the market authorisation of healthcare products in Honduras - HN. HT_DPMMT false Haiti Direction de la Pharmacie, du Médicament et de la Médecine Traditionnelle Direction de la Pharmacie, du Médicament et de la Médecine Traditionnelle manages the market authorisation of healthcare products in Haiti - HT ICCBBA false ICCBBA ICCBBA is an international non-governmental organization (NGO) that manages, develops and licenses ISBT 128; the international information standard for the terminology, coding and labelling of medical products of human origin. ICCBBA manage the allocation of globally unique identifiers to licensed facilities and maintain the ISBT 128 Standard, international databases for Facility Identification Numbers and Product Coding, supporting documentation, and educational materials. IEHPRA false Product Authorisation Number Product Authorisation Number (PA Number) as granted by the Health Products Regulatory Authority (HPRA) in Ireland. The marketing authorisation is issued with a Product Authorisation Number (PA Number) which is included on the medicine box/container in the Irish jurisdiction. INDUSTRY_ASSIGNED false Industry Assigned A unique proprietary identification number assigned by an industry sector association or other organisation, used to identify an item or service. Typically the association or organisation provides the industry sector with an identification number as key identifier of a type of trade item. INMETRO false INMETRO The National Institute of Metrology, Standardization and Industrial Quality (INMETRO) is a Brazilian federal autarchy, linked to MDIC, the Ministry of Development, Industry and Foreign Trade. INVIMA false Colombia INVIMA National Institute of Surveillance of Medications and Foods for Colombia. This organisation has developed a unique code of medications (CUM). ISBN_NUMBER false ISBN number International Standard Book Number: A unique numeric commercial book identifier. ISSN_NUMBER false ISSN number International Standard Serial Number: unique eight-digit number used to identify a print or electronic periodical publication. JFDA false Jordan Food and Drug Administration Jordan Food and Drug Administration manages the market authorisation of healthcare products in Jordan - JO JM_MOHW false Jamaica Ministry of Health and Wellness, Pharmaceutical and Regulatory Affairs (MOHW) Ministry of Health and Wellness, Pharmaceutical and Regulatory Affairs (MOHW) manages the market authorisation of healthcare products in Jamaica - JM. KZ_NCE false Kazakhstan National Center for Expertise of Medicines and Medical Devices (NCE) National Center for Expertise of Medicines and Medical Devices (NCE) manages the market authorisation of healthcare products in Kazakhstan - KZ. LMHPRA false Liberia Medicines and Health Products Regulatory Authority Liberia Medicines and Health Products Regulatory Authority manages the market authorisation of healthcare products in Liberia - LR LOTTERY_GAME_NUMBER false Lottery Game Number Unknown LOTTERY_PACK_BOOK_NUMBER false Lottery pack book number A unique identifier for a book of shrink-wrapped lottery game tickets. MANUFACTURER_PART_NUMBER Manufacturer part number or manufacturer assigned Tillverkarens artikelnummer The manufacturer’s original number. Also known as the Original Equipment Manufacturer (OEM) part number when the part is produced by a third-party manufacturer. In most cases a non-GS1 item number. Tillverkarens ursprungliga nummer. Även känt som Original Equipment Manufacturer (OEM)-artikelnummer när delen tillverkas av en tredjepartstillverkare. I de flesta fall ett icke-GS1-artikelnummer. MAPA false MAPA Brazil´s Ministério da Agricultura, Pecuária e Abastecimento, which is the Ministry of Agriculture, Livestock and Supply. MCAZ false Medicines Control Authority of Zimbabwe (MCAZ) Medicines Control Authority of Zimbabwe (MCAZ) manages the market authorisation of healthcare products in Zimbabwe - ZW MCC false South Africa Medicines Control Council (MCC) Medicines Control Council (MCC) manages the market authorisation of healthcare products in South Africa - ZA MDL false MDL The Canadian Medical Device License (MDL) is required for companies which sell Class II, III, and IV medical devices in Canada. The MDL is a product approval and should not be confused with the MDEL which is a permit for the company/distributor itself. MINSA false Nicaragua Ministerio de Salud - Direccion de Farmacias (MINSA) Ministerio de Salud - Direccion de Farmacias (MINSA) manages the market authorisation of healthcare products in Nicaragua - NI MISAU false Mozambique Departamento Farmacêutico-MISAU Departamento Farmacêutico Ministério da Saúde (MISAU) - Ministry of Health Pharmaceutical Department - manages the medicines and pharmaceutical products, including the regulation, procurement, storage, and distribution of healthcare products in Mozambique - MZ. MODEL_NUMBER Model Number Modellnummer The additional Trade Item Identification value populated by the brand owner to a base product design or specification from which a trade item is derived. The trade item inherits major features/functions from the base model and in some sectors, such as electronics or apparel. NOTE: The use of this code and value are NOT the GS1 Identification Key for Global Model Number (GMN). Modellnummer som tilldelas av varumärkesägaren. OBS! Detta är inte GS1:s identifieringsnyckel för Global Model Number (GMN). MOHSW false Ministry of Health & Social Welfare Ministry of Health & Social Welfare manages the market authorisation of healthcare products in Gambia - GM MOH_AO false Ministry of Health (MOH) Angola Ministry of Health (MOH) manages the market authorisation of healthcare products in Angola - AO MOH_BB false Ministry of Health (MOH) Barbados Ministry of Health (MOH) manages the market authorisation of healthcare products in Barbados - BB MOH_BW false Botswana Drugs Regulatory Unit (DRU) of the Ministry of Health (MOH) Drugs Regulatory Unit (DRU) of the Ministry of Health (MOH) manages the market authorisation of healthcare products in Botswana - BW MOH_GY false Ministry of Health - Guyana Ministry of Health manages the market authorisation of healthcare products in Guyana - GY MOH_MA false Ministry of Health - Morocco Ministry of Health manages the market authorisation of healthcare products in Morocco - MA MOH_MR false Mauritania Ministry of Health: Pharmacy and Laboratory Ministry of Health: Pharmacy and Laboratory manages the market authorisation of healthcare products in Mauritania - MR MOH_RW false Ministry of Health - Rwanda Ministry of Health manages the market authorisation of healthcare products in Rwanda - RW MOH_SZ false Ministry of Health (MOH) Swaziland Ministry of Health (MOH) manages the market authorisation of healthcare products in Swaziland - SZ MOH_TJ false Ministry of Health - Tajikistan Ministry of Health manages the market authorisation of healthcare products in Tajikistan - TJ MOH_TT false Trinidad and Tobago Chemistry Food and Drugs Division/Ministry of Health (CFFD/MOH) Chemistry Food and Drugs Division/Ministry of Health (CFFD/MOH) manages the market authorisation of healthcare products in Trinidad and Tobago - TT MOH_UG false Uganda National Drug Authority National Drug Authority manages the market authorisation of healthcare products in Uganda - UG MOH_UZ false Ministry of Health - Uzbekistan Ministry of Health manages the market authorisation of healthcare products in Uzbekistan - UZ MOPH_NE false Niger Ministry of Public Health Ministry of Public Health manages the market authorisation of healthcare products in Niger - NE MOPH_TD false Minister of Public Health: Direction de la Pharmacie, du Médicament et des Laboratoires Minister of Public Health: Direction de la Pharmacie, du Médicament et des Laboratoires manages the market authorisation of healthcare products in Chad - TD MRA false Medicines Regulatory Authority (MRA) Palestine Medicines Regulatory Authority (MRA) manages the market authorisation of healthcare products in Palestine, State of - PS MRA_PG false Medicines Regulatory Authority (MRA) Papua New Guinea Medicines Regulatory Authority (MRA) manages the market authorisation of healthcare products in Papua New Guinea - PG MRA_SS false Medicines Regulatory Authority (MRA) South Sudan Medicines Regulatory Authority (MRA) manages the market authorisation of healthcare products in South Sudan - SS MSD false Bolivia Unidad de Medicamentos y Tecnología en Salud (MSD) Unidad de Medicamentos y Tecnología en Salud (MSD) manages the market authorisation of healthcare products in Bolivia - BO MSP false Dominican Republic Direccion General de Drogas y Farmacias del Ministerio de Salud Pública (DGDF/MSP) Direccion General de Drogas y Farmacias del Ministerio de Salud Pública (DGDF/MSP) manages the market authorisation of healthcare products in Dominican Republic - DO MSPAS_CG false Ministère de la Santé Publique et des Affairs Sociales: Direction des Pharmacies, du Médicament et des Laboratoires Ministère de la Santé Publique et des Affairs Sociales: Direction des Pharmacies, du Médicament et des Laboratoires manages the market authorisation of healthcare products in Congo, Republic of - CG MSPAS_GT false Guatemala Ministerio de Salud Publica y Asistencia Social/Departamento de Regulación y Control de Productos Farmacéuticos y Afines (MSPAS) Ministerio de Salud Publica y Asistencia Social/Departamento de Regulación y Control de Productos Farmacéuticos y Afines (MSPAS) manages the market authorisation of healthcare products in Guatemala - GT MSPBS false Ministerio de Salud Pública y Bienestar Social (MSPBS) Ministerio de Salud Pública y Bienestar Social (MSPBS) manages the market authorisation of healthcare products in Paraguay - PY MW_PMRA false Malawi Pharmacy and Medicines Regulatory Authority (PMRA) Pharmacy and Medicines Regulatory Authority (PMRA) manages the market authorisation of healthcare products in Malawi - MW. MZ_ANARME false Mozambique National Medicines Regulatory Authority Autoridade Nacional Reguladora de Medicamento (ANARME) - National Medicines Regulatory Authority - manages the market authorisation of healthcare products in Mozambique - MZ. NABCA_PRODUCT_CODE false NABCA product code A product code issued by the National Alcohol Beverage Control Association in the United States. NADFC false National Agency of Drug and Food Control (NADFC) National Agency of Drug and Food Control (NADFC) manages the market authorisation of healthcare products in Indonesia - ID NAFDAC_NG false Nigeria National Agency for Food and Drug Administration and Control (NAFDAC) National Agency for Food and Drug Administration and Control (NAFDAC) manages the market authorisation of healthcare products in Nigeria - NG NAN Nordic Item Number Nordiskt varunummer Nordic Article Number is a 6 digit identification number needed on all human and veterinary pharmaceuticals licensed in Sweden. The number is unique for a certain packages. A NAN can be valid in one to five Nordic countries (Sweden, Denmark, Norway, Finland and Iceland) depending on if the package fulfils some basic criteria. Nordiskt varunummernummer är en sex -siffrigt identifieringsnummer som behövs på alla läkemedel som godkänts i Sverige. Numret är unikt för en viss artikel. Ett NAN kan vara giltigt i ett till fem nordiska länder: (Sverige, Danmark, Norge, Finland och Island) beroende på om artikeln uppfyller vissa grundläggande kriterier NAPALSN false National Allowance Pricing Agreement Local Stock Number National Allowance Pricing Agreement Local Stock Number is a specific identification code used within a national pricing agreement framework to track and manage inventory at a local level. NAPPI false National Pharmaceutical Product Index (NAPPI) The National Pharmaceutical Product Index or NAPPI is a comprehensive database of medical products used in South Africa. Each product has a unique NAPPI code which enables electronic data interchange throughout the health care delivery chain in South Africa. https://www.medikredit.co.za/index.php?option=com_nappi&view=nappi&Itemid=210 NCM false Kazakhstan National Center for Medicines, Medical Devices and Medical Equipment Expertise National Center for medicines, medical devices and medical equipment expertise manages the market authorisation of healthcare products in Kazakhstan - KZ NIIN false NATO Item Identification Number The NATO Item Identification Number (NIIN) (Last Nine (9) Digits of an NSN) is the fixed part of the NSN, and it remains associated with the IoS concept throughout its life cycle. However, the NSC (First Four (4) Digits) may change if there is a revision of the IoS Classification structure. NMFA false National Medicines and Food Administration National Medicines and Food Administration manages the market authorisation of healthcare products in Eritrea - ER NMPA false National Medical Products Administration (NMPA) China National Medical Products Administration. NMPB_SD false National Medicines and Poisons Board (NMPB) National Medicines and Poisons Board (NMPB) manages the market authorisation of healthcare products in Sudan - SD NMRA_LK false National Medicines Regulatory Authority (NMRA) National Medicines Regulatory Authority (NMRA) manages the market authorisation of healthcare products in Sri Lanka - LK NMRC false Namibia Medicines Regulatory Council Namibia Medicines Regulatory Council manages the market authorisation of healthcare products in Namibia - NA NPN false Natural Health Product Number (NPN) - Canada The Natural Health Product Number: Identifies the trade item as a natural health product and the number is assigned by a regulatory health organization for example the Health Canada - Natural Health Products Directorate (Health Canada). NSN false NATO Stock Number NATO Stock Number or National Stock Number is a 13-digit numeric code identifying all the standardized material items of supply as they have been recognized by all NATO countries . The complete structure of this identifier can be found at this link: https://www.nato.int/structur/AC/135/ncs_guide/english/e_1-6-5.htm NUMERO_RDN false RDN An identification number assigned by the Italian Ministry of Health to medical devices treated by the national health system NZ_MEDICINES_TERMINOLOGY_CODE false NZ Medicines Terminology Code For medicines used within NZ healthcare, the code assigned by NZULM (New Zealand List of Medicines). The NZ Medicines Terminology Code on the NZULM website is referred to as the SCTID (Snomed Concept ID). PBSL false Pharmacy Board of Sierra Leone Pharmacy Board of Sierra Leone manages the market authorisation of healthcare products in Sierra Leone - SL PCOJ false Pharmacy Council of Jamaica (PCoJ) Pharmacy Council of Jamaica (PCoJ) manages the market authorisation of healthcare products in Jamaica - JM PG_PSSB false Papua New Guinea Pharmaceutical Services Standards Branch (PSSB) Pharmaceutical Services Standards Branch (PSSB) manages the market authorisation of healthcare products in Papua New Guinea - PG. PHARMACODE_CH false Pharmacode CH A national drug code for Switzerland assigned by e-mediat AG, Bern. The identification number based on the standard Code39 and is used in the whole Swiss healthcare market. PIRC false Suriname Pharmaceutical Inspectorate and the Registration Committee Pharmaceutical Inspectorate and the Registration Committee manages the market authorisation of healthcare products in Suriname - SR PLU Price Lookup (PLU) for Variable Measure PLU-nummer A number used to indicate a price look up for a product with variable content. This is only used for items that have been assigned an industry PLU or proprietary PLU. PLU-nummer kan användas för att slå upp ett pris för en produkt med varierad vikt. Används endast för artiklar som har tilldelats antingen ett bransch- eller ett företagsspecifikt PLU. PMPB false Malawi Pharmacy, Medicines and Poisons Board Pharmacy, Medicines and Poisons Board manages the market authorisation of healthcare products in Malawi - MW PPB false Kenya Pharmacy and Poisons Board Pharmacy and Poisons Board manages the market authorisation of healthcare products in Kenya - KE PPN false Pharmacy Product Number The Pharmacy Product Number (PPN) is a globally unique identifier for pharmaceutical products, used to ensure traceability within the supply chain. It is typically encoded in a 2D data matrix on packaging and issued under the authority of the IFA (Informationsstelle für Arzneispezialitäten) as the official issuing agency. PZN false Central Pharmaceutical Number The pharmaceutical central number (Pharmazentralnummer), or PZN for short, is an identification number for the uniform identification of pharmaceuticals and medical devices subject to pharmacies available on the German market. Their assignment is carried out by the Informationsstelle für Arzneimittelspezialitäten (IFA) after an application is submitted by the manufacturer. RVG false RVG (Register Verpakte Geneesmiddelen): An identification number provided by the Institute for Drug Evaluation (College ter Beoordeling van Geneesmiddelen – CBG) in the Netherlands. This number is used as the main identification for all drugs that have been approved by the CBG for distribution within the Netherlands. RVH false RVH (Register Verpakte Homeopatische Geneesmiddelen): An identification number provided by the Institute for Drug Evaluation (College ter Beoordeling van Geneesmiddelen – CBG) in the Netherlands. This number is used as the main identification for all homeopathic drugs that have been approved by the CBG for distribution within the Netherlands. RW_FDA false Rwanda Food and Drugs Authority (FDA) Food and Drugs Authority (FDA) manages the market authorisation of healthcare products in Rwanda - RW. SA_SFDA false Saudi Food and Drug Authority (SFDA) Saudi Food and Drug Authority (SFDA) manages the market authorisation of healthcare products in Saudi Arabia - SA. SAN_4 SAN 4 Viktvarunummer A nationally set standard trade item number for a variable measure trade item. The SAN-4 is a four-digit number that uniquely identifies a weight trade item according to its country of origin. This short number is incorporated into the 13 digit GTIN symbol in combination with the weight, quantity or price. Viktvarunummer är ett nationellt nummer som unikt identifierar en artikel med variabel mått. Detta nummer ingår i streckkoden i kombination med vikt eller pris. SBDMA false Yemen Supreme Board for Drugs & Medical Appliances Supreme Board for Drugs & Medical Appliances manages the market authorisation of healthcare products in Yemen - YE SCDMTE false The Scientific Centre of Drug and Medical Technologies Expertise (SCDMTE) The Scientific Center of Drug and Medical Technologies Expertise (SCDMTE) manages the market authorisation of healthcare products in Armenia - AM SFDA false China State Food Drug Administration (SFDA) State Food Drug Administration (SFDA) manages the market authorisation of healthcare products in China - CN SG_HAS false Singapore Health Sciences Authority (HAS) Health Sciences Authority (HAS) manages the market authorisation of healthcare products in Singapore - SG. SK_SUKL false SUKL code (Slovakia) The ŠÚKL code is a unique identifier used by the State Institute for Drug Control (ŠÚKL) in Slovakia. It uniquely identifies a specific medicinal product or medical device in the ŠÚKL database. SMDC_UA false State Service of Ukraine on Medicines and Drugs Control (SMDC) State Service of Ukraine on Medicines and Drugs Control (SMDC) manages the market authorisation of healthcare products in Ukraine - UA SN_DPM false Senegal La Direction de la Pharmacie et du Médicament (DPM) La Direction de la Pharmacie et du Médicament (DPM) manages the market authorisation of healthcare products in Senegal - SN. SRAMA false State Regulatory Agency for Medical Activities State Regulatory Agency for Medical Activities manages the market authorisation of healthcare products in Georgia - GE SS_MOH false South Sudan Ministry of Health (MOH) - Republic of South Sudan (RSS) The Ministry of Health (MOH) Drug & Food Control Authority manages the market authorization of healthcare products in South Sudan -SS. SUPPLIER_ASSIGNED Supplier Assigned Leverantörsartikelnummer The additional Trade Item Identification value populated by the supplier in most cases a non-GS1 item number. Artikelnummer som tilldelas av leverantören, i de flesta fall ett icke-GS1-artikelnummer. SWISSMEDIC_NUMBER false Swissmedic Number Every drug authorised in Switzerland is assigned such a number when it is authorised. The Swissmedic number must be printed on the package. The Swiss Medic number is a market authorization number. SZ_MOH false Ministry of Health (MOH) Eswatini Ministry of Health (MOH) manages the market authorisation of healthcare products in Eswatini - SZ. TFDA false Tanzania Food and Drugs Authority (TFDA) Tanzania Food and Drugs Authority (TFDA) manages the market authorisation of healthcare products in Tanzania - TZ TG_DPML false Togo Direction de la pharmacie, du Médicament et des Laboratoires (DPML) Direction de la pharmacie, du Médicament et des Laboratoires (DPML) manages the market authorisation of healthcare products in Togo - TG. TZ_TMDA false Tanzania Medicines & Medical Devices Authority (TMDA) Tanzania Medicines & Medical Devices Authority (TMDA) manages the market authorisation of healthcare products in Tanzania - TZ. UG_NDA false Uganda National Drug Authority (NDA) National Drug Authority (NDA) manages the market authorisation of healthcare products in Uganda - UG. US_CMS_NDC false US Centers for Medicare and Medicaid Services National Drug Code This derivative of the National Drug Code (NDC) was created and is utilized by the Centers for Medicare and Medicaid Services(CMS). The Health Insurance Portability and Accountability Act (HIPAA) standard code set expects the NDC to be expressed in a 5-4-2 configuration. When necessary, a zero (“0”) will pad the labeler, product, or package code segments of the FDA NDC to ensure a fixed length in the 5-4-2 configuration. The CMS NDC, of uniform code length, is referenced in lists and databases of additional US government agencies (such as the UMLS) in place of the FDA NDC. US_FDA_NDC false US Federal Food, Drug National Drug Code The National Drug Code (NDC) of the United States of America is a unique 3-segment number, including dashes, assigned to each medication listed under Section 510 of the U.S. Federal, Food, Drug, and Cosmetics Act. This combination of numeric segments representing the labeler or vendor, product, and trade package size is the principal identifier for medications in the eyes of the U.S. Food and Drug Administration (FDA). WAND_NUMBER false WAND Number The identification code assigned from the WAND (Web Assisted Notification of Devices) database. WHOPQN false WHO PreQualification Number The World Health Organization’s Prequalification ensures active pharmaceutical ingredients (APIs) and finished pharmaceutical products (FPPs) are safe, appropriate and meet stringent quality standards. In addition to medicines, WHO prequalification also covers in vitro diagnostics, vaccines and vector control products. https://extranet.who.int/prequal/content/what-we-do ZAMRA false Zambia Medicines Regulatory Authority (ZAMRA) Zambia Medicines Regulatory Authority (ZAMRA) manages the market authorisation of healthcare products in Zambia - ZM Z_INDEX false Z INDEX An additional identification number used to identify all medical supplies and drugs in the Netherlands when managing reimbursements for the items. The Z-Index number is assigned to every product by Z-Index, which is a regulatory body in the Netherlands for the healthcare industry.