01 1Siegfried AG
01 1RESCINNAMINE
01 1Switzerland
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 284
Submission : 1957-12-18
Status : Inactive
Type : II
A Rescinnamine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Rescinnamine, including repackagers and relabelers. The FDA regulates Rescinnamine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Rescinnamine 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 Rescinnamine supplier is an individual or a company that provides Rescinnamine active pharmaceutical ingredient (API) or Rescinnamine finished formulations upon request. The Rescinnamine suppliers may include Rescinnamine API manufacturers, exporters, distributors and traders.
click here to find a list of Rescinnamine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Rescinnamine DMF (Drug Master File) is a document detailing the whole manufacturing process of Rescinnamine active pharmaceutical ingredient (API) in detail. Different forms of Rescinnamine DMFs exist exist since differing nations have different regulations, such as Rescinnamine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Rescinnamine DMF submitted to regulatory agencies in the US is known as a USDMF. Rescinnamine USDMF includes data on Rescinnamine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Rescinnamine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Rescinnamine suppliers with USDMF on PharmaCompass.
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