01 1Urquima S.A. Grupo Uriach
01 1FLUTRIMAZOLE
01 1Spain
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 12806
Submission : 1997-12-24
Status : Inactive
Type : II
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A Flutrimazole manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Flutrimazole, including repackagers and relabelers. The FDA regulates Flutrimazole manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Flutrimazole 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 Flutrimazole manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Flutrimazole supplier is an individual or a company that provides Flutrimazole active pharmaceutical ingredient (API) or Flutrimazole finished formulations upon request. The Flutrimazole suppliers may include Flutrimazole API manufacturers, exporters, distributors and traders.
click here to find a list of Flutrimazole suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Flutrimazole DMF (Drug Master File) is a document detailing the whole manufacturing process of Flutrimazole active pharmaceutical ingredient (API) in detail. Different forms of Flutrimazole DMFs exist exist since differing nations have different regulations, such as Flutrimazole USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Flutrimazole DMF submitted to regulatory agencies in the US is known as a USDMF. Flutrimazole USDMF includes data on Flutrimazole's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Flutrimazole USDMF is kept confidential to protect the manufacturer’s intellectual property.
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