Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
01 1Sanofi
02 1Gedeon Richter
03 2Merck & Co
04 1ScinoPharm Taiwan Ltd
05 1Blank
01 1IDENTIFICATION, ASSAY & SPECIFICATION FOR MESTRANOL
02 4MESTRANOL
03 1MESTRANOL USP
01 1France
02 1Hungary
03 1Taiwan
04 2U.S.A
05 1Blank
01 6Inactive
01 6Blank
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 : 1614
Submission : 1970-11-18
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5744
Submission : 1985-02-28
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 901
Submission : 1965-07-22
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3951
Submission : 1980-09-22
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 17066
Submission : 2003-12-31
Status : Inactive
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 1174
Submission : 1968-04-24
Status : Inactive
Type : II
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PharmaCompass offers a list of Mestranol API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Mestranol manufacturer or Mestranol supplier for your needs.
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A EE3-ME manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of EE3-ME, including repackagers and relabelers. The FDA regulates EE3-ME manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. EE3-ME API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A EE3-ME supplier is an individual or a company that provides EE3-ME active pharmaceutical ingredient (API) or EE3-ME finished formulations upon request. The EE3-ME suppliers may include EE3-ME API manufacturers, exporters, distributors and traders.
click here to find a list of EE3-ME suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A EE3-ME DMF (Drug Master File) is a document detailing the whole manufacturing process of EE3-ME active pharmaceutical ingredient (API) in detail. Different forms of EE3-ME DMFs exist exist since differing nations have different regulations, such as EE3-ME USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A EE3-ME DMF submitted to regulatory agencies in the US is known as a USDMF. EE3-ME USDMF includes data on EE3-ME's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The EE3-ME USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of EE3-ME suppliers with USDMF on PharmaCompass.
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