Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
01 1SANOFI CHIMIE Gentilly FR
02 1Hebei Huarong Pharmaceutical Co Ltd Shijiazhuang CN
03 1Hebei Huarong Pharmaceutical Co Ltd Xingtai CN
04 1MEIJI SEIKA PHARMA CO., LTD. Tokyo JP
05 1NINGXIA KINGVIT PHARMACEUTICAL CO., LTD. YinChuan CN
06 1North China Pharmaceutical Victor Co. LTD Shijiazhuang CN
07 1YUXING BIOTECHNOLOGY (GROUP) CO.,LTD. Ningjin CN
01 6Cyanocobalamin
02 1Cyanocobalamin, Aerobic production line
01 5China
02 1France
03 1Japan
01 1Expired
02 3Valid
03 3Withdrawn by Holder
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Certificate Number : R1-CEP 1998-056 - Rev 05
Status : Withdrawn by Holder
Issue Date : 2009-10-23
Type : Chemical
Substance Number : 547
Certificate Number : R1-CEP 2008-070 - Rev 03
Status : Valid
Issue Date : 2021-04-23
Type : Chemical
Substance Number : 547
Cyanocobalamin, Aerobic Production Line
Certificate Number : CEP 2011-205 - Rev 03
Status : Valid
Issue Date : 2024-07-16
Type : Chemical
Substance Number : 547
Certificate Number : R1-CEP 2003-233 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2010-09-23
Type : Chemical
Substance Number : 547
Certificate Number : R0-CEP 2004-293 - Rev 01
Status : Expired
Issue Date : 2011-05-26
Type : Chemical
Substance Number : 547
Certificate Number : R1-CEP 2014-172 - Rev 00
Status : Valid
Issue Date : 2022-03-29
Type : Chemical
Substance Number : 547
Certificate Number : R1-CEP 2006-204 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2014-12-05
Type : Chemical
Substance Number : 547
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.
A Vitamin B12 CEP of the European Pharmacopoeia monograph is often referred to as a Vitamin B12 Certificate of Suitability (COS). The purpose of a Vitamin B12 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Vitamin B12 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Vitamin B12 to their clients by showing that a Vitamin B12 CEP has been issued for it. The manufacturer submits a Vitamin B12 CEP (COS) as part of the market authorization procedure, and it takes on the role of a Vitamin B12 CEP holder for the record. Additionally, the data presented in the Vitamin B12 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Vitamin B12 DMF.
A Vitamin B12 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Vitamin B12 CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Vitamin B12 suppliers with CEP (COS) on PharmaCompass.
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