01 1RHODIA INC US 08512-7500 Cranbury
01 1CLOREXOLONE
01 1U.S.A
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 951
Submission : 1966-03-30
Status : Inactive
Type : II
A Clorexolone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Clorexolone, including repackagers and relabelers. The FDA regulates Clorexolone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Clorexolone 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 Clorexolone supplier is an individual or a company that provides Clorexolone active pharmaceutical ingredient (API) or Clorexolone finished formulations upon request. The Clorexolone suppliers may include Clorexolone API manufacturers, exporters, distributors and traders.
click here to find a list of Clorexolone suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Clorexolone DMF (Drug Master File) is a document detailing the whole manufacturing process of Clorexolone active pharmaceutical ingredient (API) in detail. Different forms of Clorexolone DMFs exist exist since differing nations have different regulations, such as Clorexolone USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Clorexolone DMF submitted to regulatory agencies in the US is known as a USDMF. Clorexolone USDMF includes data on Clorexolone's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Clorexolone USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Clorexolone suppliers with USDMF on PharmaCompass.
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