Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
01 1Sanofi
02 1OLTA PHARMACEUTICALS CORP
01 1LINDANE
02 1LINDANE, USP
01 1France
02 1U.S.A
01 2Inactive
01 2Blank
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 : 8167
Submission : 1989-08-15
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 22259
Submission : 2009-01-08
Status : Inactive
Type : II
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PharmaCompass offers a list of gamma-BHC 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 gamma-BHC manufacturer or gamma-BHC supplier for your needs.
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PharmaCompass also assists you with knowing the gamma-BHC API Price utilized in the formulation of products. gamma-BHC API Price is not always fixed or binding as the gamma-BHC Price is obtained through a variety of data sources. The gamma-BHC Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A AKOS024390982 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AKOS024390982, including repackagers and relabelers. The FDA regulates AKOS024390982 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AKOS024390982 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 AKOS024390982 supplier is an individual or a company that provides AKOS024390982 active pharmaceutical ingredient (API) or AKOS024390982 finished formulations upon request. The AKOS024390982 suppliers may include AKOS024390982 API manufacturers, exporters, distributors and traders.
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A AKOS024390982 DMF (Drug Master File) is a document detailing the whole manufacturing process of AKOS024390982 active pharmaceutical ingredient (API) in detail. Different forms of AKOS024390982 DMFs exist exist since differing nations have different regulations, such as AKOS024390982 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A AKOS024390982 DMF submitted to regulatory agencies in the US is known as a USDMF. AKOS024390982 USDMF includes data on AKOS024390982's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The AKOS024390982 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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