01 1Sumitomo Chemical
01 1SUMITHRIN
01 1Japan
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5631
Submission : 1984-11-30
Status : Inactive
Type : II
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PharmaCompass offers a list of Phenothrin 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 Phenothrin manufacturer or Phenothrin supplier for your needs.
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A Fenotrina manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fenotrina, including repackagers and relabelers. The FDA regulates Fenotrina manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fenotrina 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 Fenotrina supplier is an individual or a company that provides Fenotrina active pharmaceutical ingredient (API) or Fenotrina finished formulations upon request. The Fenotrina suppliers may include Fenotrina API manufacturers, exporters, distributors and traders.
click here to find a list of Fenotrina suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Fenotrina DMF (Drug Master File) is a document detailing the whole manufacturing process of Fenotrina active pharmaceutical ingredient (API) in detail. Different forms of Fenotrina DMFs exist exist since differing nations have different regulations, such as Fenotrina USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Fenotrina DMF submitted to regulatory agencies in the US is known as a USDMF. Fenotrina USDMF includes data on Fenotrina's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Fenotrina USDMF is kept confidential to protect the manufacturer’s intellectual property.
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