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01 1NICERGOLINE
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01 1Inactive
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USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 8266
Submission : 1989-10-17
Status : Inactive
Type : II
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A Nicergoline manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nicergoline, including repackagers and relabelers. The FDA regulates Nicergoline manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nicergoline 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 Nicergoline manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Nicergoline supplier is an individual or a company that provides Nicergoline active pharmaceutical ingredient (API) or Nicergoline finished formulations upon request. The Nicergoline suppliers may include Nicergoline API manufacturers, exporters, distributors and traders.
click here to find a list of Nicergoline suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Nicergoline DMF (Drug Master File) is a document detailing the whole manufacturing process of Nicergoline active pharmaceutical ingredient (API) in detail. Different forms of Nicergoline DMFs exist exist since differing nations have different regulations, such as Nicergoline USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Nicergoline DMF submitted to regulatory agencies in the US is known as a USDMF. Nicergoline USDMF includes data on Nicergoline's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Nicergoline USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Nicergoline suppliers with USDMF on PharmaCompass.
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