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01 1CIPROCINONIDE-MANUF BY SYNTEX RES IN CA, BAHAMAS CHEM DIV SYNTEX
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01 1Inactive
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USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3172
Submission : 1978-03-23
Status : Inactive
Type : II
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A Ciprocinonide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ciprocinonide, including repackagers and relabelers. The FDA regulates Ciprocinonide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ciprocinonide 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 Ciprocinonide supplier is an individual or a company that provides Ciprocinonide active pharmaceutical ingredient (API) or Ciprocinonide finished formulations upon request. The Ciprocinonide suppliers may include Ciprocinonide API manufacturers, exporters, distributors and traders.
click here to find a list of Ciprocinonide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Ciprocinonide DMF (Drug Master File) is a document detailing the whole manufacturing process of Ciprocinonide active pharmaceutical ingredient (API) in detail. Different forms of Ciprocinonide DMFs exist exist since differing nations have different regulations, such as Ciprocinonide USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Ciprocinonide DMF submitted to regulatory agencies in the US is known as a USDMF. Ciprocinonide USDMF includes data on Ciprocinonide's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Ciprocinonide USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Ciprocinonide suppliers with USDMF on PharmaCompass.
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