01 1Dishman Carbogen Amcis
01 1CETRIMIDE
01 1India
01 1Active
01 1Complete
GDUFA
DMF Review : Complete
Rev. Date : 2021-02-26
Pay. Date : 2020-11-25
DMF Number : 35282
Submission : 2020-11-02
Status : Active
Type : II
A Cetrimide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cetrimide, including repackagers and relabelers. The FDA regulates Cetrimide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cetrimide 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 Cetrimide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cetrimide supplier is an individual or a company that provides Cetrimide active pharmaceutical ingredient (API) or Cetrimide finished formulations upon request. The Cetrimide suppliers may include Cetrimide API manufacturers, exporters, distributors and traders.
click here to find a list of Cetrimide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cetrimide DMF (Drug Master File) is a document detailing the whole manufacturing process of Cetrimide active pharmaceutical ingredient (API) in detail. Different forms of Cetrimide DMFs exist exist since differing nations have different regulations, such as Cetrimide USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Cetrimide DMF submitted to regulatory agencies in the US is known as a USDMF. Cetrimide USDMF includes data on Cetrimide's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Cetrimide USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Cetrimide suppliers with USDMF on PharmaCompass.
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