01 1elm-plastic GmbH
01 1EMETINE HCL INJECTION
01 1Germany
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2820
Submission : 1977-01-25
Status : Inactive
Type : II
A Emetine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Emetine, including repackagers and relabelers. The FDA regulates Emetine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Emetine 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 Emetine supplier is an individual or a company that provides Emetine active pharmaceutical ingredient (API) or Emetine finished formulations upon request. The Emetine suppliers may include Emetine API manufacturers, exporters, distributors and traders.
click here to find a list of Emetine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Emetine DMF (Drug Master File) is a document detailing the whole manufacturing process of Emetine active pharmaceutical ingredient (API) in detail. Different forms of Emetine DMFs exist exist since differing nations have different regulations, such as Emetine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Emetine DMF submitted to regulatory agencies in the US is known as a USDMF. Emetine USDMF includes data on Emetine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Emetine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Emetine suppliers with USDMF on PharmaCompass.
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