01 1Dishman Carbogen Amcis
01 1HEXETIDINE
01 1India
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 24162
Submission : 2010-09-07
Status : Inactive
Type : II
A Hexetidine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hexetidine, including repackagers and relabelers. The FDA regulates Hexetidine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hexetidine 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 Hexetidine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Hexetidine supplier is an individual or a company that provides Hexetidine active pharmaceutical ingredient (API) or Hexetidine finished formulations upon request. The Hexetidine suppliers may include Hexetidine API manufacturers, exporters, distributors and traders.
click here to find a list of Hexetidine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Hexetidine DMF (Drug Master File) is a document detailing the whole manufacturing process of Hexetidine active pharmaceutical ingredient (API) in detail. Different forms of Hexetidine DMFs exist exist since differing nations have different regulations, such as Hexetidine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Hexetidine DMF submitted to regulatory agencies in the US is known as a USDMF. Hexetidine USDMF includes data on Hexetidine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Hexetidine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Hexetidine suppliers with USDMF on PharmaCompass.
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