Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
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01 1Sanofi
02 1OLTA PHARMACEUTICALS CORP
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01 1LINDANE
02 1LINDANE, USP
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01 1France
02 1U.S.A
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01 2Inactive
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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 Lacco HI lin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lacco HI lin, including repackagers and relabelers. The FDA regulates Lacco HI lin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lacco HI lin 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 Lacco HI lin supplier is an individual or a company that provides Lacco HI lin active pharmaceutical ingredient (API) or Lacco HI lin finished formulations upon request. The Lacco HI lin suppliers may include Lacco HI lin API manufacturers, exporters, distributors and traders.
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A Lacco HI lin DMF (Drug Master File) is a document detailing the whole manufacturing process of Lacco HI lin active pharmaceutical ingredient (API) in detail. Different forms of Lacco HI lin DMFs exist exist since differing nations have different regulations, such as Lacco HI lin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Lacco HI lin DMF submitted to regulatory agencies in the US is known as a USDMF. Lacco HI lin USDMF includes data on Lacco HI lin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Lacco HI lin USDMF is kept confidential to protect the manufacturer’s intellectual property.
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