EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 1EUROAPI FRANCE
02 1Interquim, S.A. de C.V.
03 1Sanofi Winthrop Industrie
04 1NURAY CHEMICALS PRIVATE LIMITED
05 1Supriya Lifescience Limited
06 1Professional Compounding Centers of America dba PCCA
07 2Spectrum Laboratory Products, Inc.
01 1HYDROXOCOBALAMIN
02 6Hydroxocobalamin
03 1Hydroxocobalamin VITAMIN B12a
01 2France
02 2India
03 1Spain
04 2U.S.A
05 1United Kingdom
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
NDC Package Code : 82298-921
Start Marketing Date : 2015-02-01
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 : 40074-0011
Start Marketing Date : 2022-02-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
NDC Package Code : 50396-7902
Start Marketing Date : 2015-02-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
NDC Package Code : 58159-027
Start Marketing Date : 2019-10-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (5kg/5kg)
Marketing Category : BULK INGREDIENT
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
NDC Package Code : 61281-9600
Start Marketing Date : 2017-02-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-5046
Start Marketing Date : 2018-11-06
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 49452-3622
Start Marketing Date : 2021-03-16
End Marketing Date : 2025-06-30
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49452-3623
Start Marketing Date : 1998-06-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
A Hydroxocobalamin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hydroxocobalamin, including repackagers and relabelers. The FDA regulates Hydroxocobalamin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hydroxocobalamin 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 Hydroxocobalamin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Hydroxocobalamin supplier is an individual or a company that provides Hydroxocobalamin active pharmaceutical ingredient (API) or Hydroxocobalamin finished formulations upon request. The Hydroxocobalamin suppliers may include Hydroxocobalamin API manufacturers, exporters, distributors and traders.
click here to find a list of Hydroxocobalamin 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 Hydroxocobalamin as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Hydroxocobalamin 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 Hydroxocobalamin 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 Hydroxocobalamin and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Hydroxocobalamin NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Hydroxocobalamin suppliers with NDC on PharmaCompass.
We have 7 companies offering Hydroxocobalamin
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