01 1Gyma Laboratories of America
01 1CHLORPHENTERMINE HCL
01 1U.S.A
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2143
Submission : 1973-08-21
Status : Inactive
Type : II
A Chlorphentermine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Chlorphentermine, including repackagers and relabelers. The FDA regulates Chlorphentermine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Chlorphentermine 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 Chlorphentermine supplier is an individual or a company that provides Chlorphentermine active pharmaceutical ingredient (API) or Chlorphentermine finished formulations upon request. The Chlorphentermine suppliers may include Chlorphentermine API manufacturers, exporters, distributors and traders.
click here to find a list of Chlorphentermine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Chlorphentermine DMF (Drug Master File) is a document detailing the whole manufacturing process of Chlorphentermine active pharmaceutical ingredient (API) in detail. Different forms of Chlorphentermine DMFs exist exist since differing nations have different regulations, such as Chlorphentermine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Chlorphentermine DMF submitted to regulatory agencies in the US is known as a USDMF. Chlorphentermine USDMF includes data on Chlorphentermine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Chlorphentermine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Chlorphentermine suppliers with USDMF on PharmaCompass.
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