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