01 1Eli Lilly
01 1CHLORMADINONE ACETATE PREMIX (VET) MADE PART OF D-699V
01 1U.S.A
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 704
Submission : 1963-08-05
Status : Inactive
Type : II
22
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A Traslan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Traslan, including repackagers and relabelers. The FDA regulates Traslan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Traslan API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Traslan manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Traslan supplier is an individual or a company that provides Traslan active pharmaceutical ingredient (API) or Traslan finished formulations upon request. The Traslan suppliers may include Traslan API manufacturers, exporters, distributors and traders.
click here to find a list of Traslan suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Traslan DMF (Drug Master File) is a document detailing the whole manufacturing process of Traslan active pharmaceutical ingredient (API) in detail. Different forms of Traslan DMFs exist exist since differing nations have different regulations, such as Traslan USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Traslan DMF submitted to regulatory agencies in the US is known as a USDMF. Traslan USDMF includes data on Traslan's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Traslan USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Traslan suppliers with USDMF on PharmaCompass.
