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