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