01 1Fine Organics
01 1ETINTIDINE HYDROCHLORIDE
01 1United Kingdom
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5692
Submission : 1985-01-28
Status : Inactive
Type : II
A Etintidine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Etintidine, including repackagers and relabelers. The FDA regulates Etintidine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Etintidine 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 Etintidine supplier is an individual or a company that provides Etintidine active pharmaceutical ingredient (API) or Etintidine finished formulations upon request. The Etintidine suppliers may include Etintidine API manufacturers, exporters, distributors and traders.
click here to find a list of Etintidine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Etintidine DMF (Drug Master File) is a document detailing the whole manufacturing process of Etintidine active pharmaceutical ingredient (API) in detail. Different forms of Etintidine DMFs exist exist since differing nations have different regulations, such as Etintidine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Etintidine DMF submitted to regulatory agencies in the US is known as a USDMF. Etintidine USDMF includes data on Etintidine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Etintidine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Etintidine suppliers with USDMF on PharmaCompass.
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