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01 1THIETHYLPERAZONE MALATE
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01 1Inactive
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USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 7813
Submission : 1988-12-20
Status : Inactive
Type : II
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A Thiethylperazine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Thiethylperazine, including repackagers and relabelers. The FDA regulates Thiethylperazine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Thiethylperazine 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 Thiethylperazine supplier is an individual or a company that provides Thiethylperazine active pharmaceutical ingredient (API) or Thiethylperazine finished formulations upon request. The Thiethylperazine suppliers may include Thiethylperazine API manufacturers, exporters, distributors and traders.
click here to find a list of Thiethylperazine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Thiethylperazine DMF (Drug Master File) is a document detailing the whole manufacturing process of Thiethylperazine active pharmaceutical ingredient (API) in detail. Different forms of Thiethylperazine DMFs exist exist since differing nations have different regulations, such as Thiethylperazine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Thiethylperazine DMF submitted to regulatory agencies in the US is known as a USDMF. Thiethylperazine USDMF includes data on Thiethylperazine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Thiethylperazine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Thiethylperazine suppliers with USDMF on PharmaCompass.
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