Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
01 1Sanofi
01 1MEPHENTERMINE (BASE & SULFATE)
01 1France
01 1Inactive
01 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 : 5439
Submission : 1984-06-29
Status : Inactive
Type : II
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PharmaCompass offers a list of Mephentermine 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 Mephentermine manufacturer or Mephentermine supplier for your needs.
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PharmaCompass also assists you with knowing the Mephentermine API Price utilized in the formulation of products. Mephentermine API Price is not always fixed or binding as the Mephentermine Price is obtained through a variety of data sources. The Mephentermine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Wyamine Sulfatereg manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Wyamine Sulfatereg, including repackagers and relabelers. The FDA regulates Wyamine Sulfatereg manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Wyamine Sulfatereg 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 Wyamine Sulfatereg supplier is an individual or a company that provides Wyamine Sulfatereg active pharmaceutical ingredient (API) or Wyamine Sulfatereg finished formulations upon request. The Wyamine Sulfatereg suppliers may include Wyamine Sulfatereg API manufacturers, exporters, distributors and traders.
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A Wyamine Sulfatereg DMF (Drug Master File) is a document detailing the whole manufacturing process of Wyamine Sulfatereg active pharmaceutical ingredient (API) in detail. Different forms of Wyamine Sulfatereg DMFs exist exist since differing nations have different regulations, such as Wyamine Sulfatereg USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Wyamine Sulfatereg DMF submitted to regulatory agencies in the US is known as a USDMF. Wyamine Sulfatereg USDMF includes data on Wyamine Sulfatereg's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Wyamine Sulfatereg USDMF is kept confidential to protect the manufacturer’s intellectual property.
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