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01 1SANOFI CHIMIE
02 1SANOFI WINTHROP INDUSTRIE
03 1Hebei Hualong Pharmaceutical Co. , Ltd.
04 1Interquim, S. A. de C. V.
01 1Acetic acid hydroxocobalamin
02 1Hydroxocobalamin acetate
03 1Hydroxocobalamin acetate
04 1Hydroxocobalamin actate
01 1China
02 2France
03 1Mexico
Registration Number : 218MF10374
Registrant's Address : 82 Avenue Raspail 94250 Gentilly France
Initial Date of Registration : 2006-03-20
Latest Date of Registration : 2013-10-09
Hydroxocobalamin acetate "Sanofi"
Registration Number : 225MF10128
Registrant's Address : 82 Avenue Raspail 94250 Gentilly France
Initial Date of Registration : 2013-07-09
Latest Date of Registration : 2013-07-09
Registration Number : 304MF10067
Registrant's Address : No. 8, Weier Road, Ningjin Salinization Industrial Park, Xingtai, Hebei Province, Chi...
Initial Date of Registration : 2022-04-20
Latest Date of Registration : 2022-04-20
Registration Number : 226MF10035
Registrant's Address : Av. Antoine Lavoisier #22, Fracc. Parque Industrial Cuamatla 54730 Cuautitla(')n Izca...
Initial Date of Registration : 2014-02-05
Latest Date of Registration : 2014-02-05
A Hydroxocobalamin Acetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hydroxocobalamin Acetate, including repackagers and relabelers. The FDA regulates Hydroxocobalamin Acetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hydroxocobalamin Acetate 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 Acetate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Hydroxocobalamin Acetate supplier is an individual or a company that provides Hydroxocobalamin Acetate active pharmaceutical ingredient (API) or Hydroxocobalamin Acetate finished formulations upon request. The Hydroxocobalamin Acetate suppliers may include Hydroxocobalamin Acetate API manufacturers, exporters, distributors and traders.
click here to find a list of Hydroxocobalamin Acetate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Hydroxocobalamin Acetate Drug Master File in Japan (Hydroxocobalamin Acetate JDMF) empowers Hydroxocobalamin Acetate API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Hydroxocobalamin Acetate JDMF during the approval evaluation for pharmaceutical products. At the time of Hydroxocobalamin Acetate JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Hydroxocobalamin Acetate suppliers with JDMF on PharmaCompass.
We have 3 companies offering Hydroxocobalamin Acetate
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