01 1HUANGSHI MEIFENG CHEMICAL CO LTD
01 1SULISOBENZONE
01 1China
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 23451
Submission : 2010-01-11
Status : Inactive
Type : II
A Sulisobenzone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sulisobenzone, including repackagers and relabelers. The FDA regulates Sulisobenzone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sulisobenzone 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 Sulisobenzone supplier is an individual or a company that provides Sulisobenzone active pharmaceutical ingredient (API) or Sulisobenzone finished formulations upon request. The Sulisobenzone suppliers may include Sulisobenzone API manufacturers, exporters, distributors and traders.
click here to find a list of Sulisobenzone suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Sulisobenzone DMF (Drug Master File) is a document detailing the whole manufacturing process of Sulisobenzone active pharmaceutical ingredient (API) in detail. Different forms of Sulisobenzone DMFs exist exist since differing nations have different regulations, such as Sulisobenzone USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Sulisobenzone DMF submitted to regulatory agencies in the US is known as a USDMF. Sulisobenzone USDMF includes data on Sulisobenzone's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Sulisobenzone USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Sulisobenzone suppliers with USDMF on PharmaCompass.
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