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