01 1Procos
01 1ALVERINE CITRATE
01 1Italy
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 29917
Submission : 2015-10-06
Status : Inactive
Type : II
A Alverine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Alverine, including repackagers and relabelers. The FDA regulates Alverine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Alverine 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 Alverine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Alverine supplier is an individual or a company that provides Alverine active pharmaceutical ingredient (API) or Alverine finished formulations upon request. The Alverine suppliers may include Alverine API manufacturers, exporters, distributors and traders.
click here to find a list of Alverine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Alverine DMF (Drug Master File) is a document detailing the whole manufacturing process of Alverine active pharmaceutical ingredient (API) in detail. Different forms of Alverine DMFs exist exist since differing nations have different regulations, such as Alverine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Alverine DMF submitted to regulatory agencies in the US is known as a USDMF. Alverine USDMF includes data on Alverine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Alverine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Alverine suppliers with USDMF on PharmaCompass.
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