Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
01 1Sanofi
02 1Aspen API
03 1Bayer AG
04 1Fareva
05 1Fujifilm Diosynth Biotechnologies
06 1Lupin Ltd
07 1Medimpex
08 1Merck & Co
09 1Mitsubishi Corporation
10 1Naari
11 1Novo Nordisk
12 1Blank
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 1846
Submission : 1971-12-22
Status :
Type : II
Aspen API. More than just an API™
GDUFA
DMF Review : Complete
Rev. Date : 2012-12-26
Pay. Date : 2012-11-14
DMF Number : 10185
Submission : 1993-04-12
Status :
Type : II
89
PharmaCompass offers a list of Norethisterone Acetate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Norethisterone Acetate manufacturer or Norethisterone Acetate supplier for your needs.
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A LO-BLISOVI FE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of LO-BLISOVI FE, including repackagers and relabelers. The FDA regulates LO-BLISOVI FE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. LO-BLISOVI FE API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A LO-BLISOVI FE supplier is an individual or a company that provides LO-BLISOVI FE active pharmaceutical ingredient (API) or LO-BLISOVI FE finished formulations upon request. The LO-BLISOVI FE suppliers may include LO-BLISOVI FE API manufacturers, exporters, distributors and traders.
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A LO-BLISOVI FE DMF (Drug Master File) is a document detailing the whole manufacturing process of LO-BLISOVI FE active pharmaceutical ingredient (API) in detail. Different forms of LO-BLISOVI FE DMFs exist exist since differing nations have different regulations, such as LO-BLISOVI FE USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A LO-BLISOVI FE DMF submitted to regulatory agencies in the US is known as a USDMF. LO-BLISOVI FE USDMF includes data on LO-BLISOVI FE's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The LO-BLISOVI FE USDMF is kept confidential to protect the manufacturer’s intellectual property.
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We have 11 companies offering LO-BLISOVI FE
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