01 1Siegfried AG
01 1XIPAMIDE
01 1Switzerland
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2776
Submission : 1976-10-01
Status : Inactive
Type : II
A Xipamide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Xipamide, including repackagers and relabelers. The FDA regulates Xipamide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Xipamide 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 Xipamide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Xipamide supplier is an individual or a company that provides Xipamide active pharmaceutical ingredient (API) or Xipamide finished formulations upon request. The Xipamide suppliers may include Xipamide API manufacturers, exporters, distributors and traders.
click here to find a list of Xipamide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Xipamide DMF (Drug Master File) is a document detailing the whole manufacturing process of Xipamide active pharmaceutical ingredient (API) in detail. Different forms of Xipamide DMFs exist exist since differing nations have different regulations, such as Xipamide USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Xipamide DMF submitted to regulatory agencies in the US is known as a USDMF. Xipamide USDMF includes data on Xipamide's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Xipamide USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Xipamide suppliers with USDMF on PharmaCompass.
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