EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 4EUROAPI FRANCE
02 1Interquim, S.A. de C.V.
03 1Sanofi chimie
04 1DSM Nutritional Products Ltd.
05 1Hebei Huarong Pharmaceutical Co., Ltd.
06 1Medisca Inc.
07 1Spectrum Laboratory Products, Inc.
08 2Willow Birch Pharma Inc.
01 5CYANOCOBALAMIN
02 1CYANOCOBALAMINE
03 6Cyanocobalamin
01 1China
02 5France
03 1Netherlands
04 1Spain
05 4U.S.A
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
NDC Package Code : 82298-201
Start Marketing Date : 2011-06-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
Interquim comes from an international group of 50 companies active in the pharma, hospital, diagnostics, fine chemicals & feed sectors.
NDC Package Code : 40074-0013
Start Marketing Date : 2022-02-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
NDC Package Code : 50396-7800
Start Marketing Date : 2011-06-29
End Marketing Date : 2026-08-15
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
NDC Package Code : 82298-202
Start Marketing Date : 2011-06-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
NDC Package Code : 82298-203
Start Marketing Date : 2011-06-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
NDC Package Code : 82298-204
Start Marketing Date : 2011-06-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 43225-1001
Start Marketing Date : 2022-09-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-3310
Start Marketing Date : 2024-06-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 10695-172
Start Marketing Date : 2024-08-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 10695-172
Start Marketing Date : 2024-08-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
A Vitamin B12 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vitamin B12, including repackagers and relabelers. The FDA regulates Vitamin B12 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vitamin B12 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Vitamin B12 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Vitamin B12 supplier is an individual or a company that provides Vitamin B12 active pharmaceutical ingredient (API) or Vitamin B12 finished formulations upon request. The Vitamin B12 suppliers may include Vitamin B12 API manufacturers, exporters, distributors and traders.
click here to find a list of Vitamin B12 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Vitamin B12 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Vitamin B12 API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Vitamin B12 as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Vitamin B12 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Vitamin B12 NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Vitamin B12 suppliers with NDC on PharmaCompass.
We have 8 companies offering Vitamin B12
Get in contact with the supplier of your choice:
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