01 1Abbott Laboratories
01 1ETHCHLORVYNOL
01 1U.S.A
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4782
Submission : 1982-12-27
Status : Inactive
Type : II
A Ethchlorvynol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ethchlorvynol, including repackagers and relabelers. The FDA regulates Ethchlorvynol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ethchlorvynol 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 Ethchlorvynol supplier is an individual or a company that provides Ethchlorvynol active pharmaceutical ingredient (API) or Ethchlorvynol finished formulations upon request. The Ethchlorvynol suppliers may include Ethchlorvynol API manufacturers, exporters, distributors and traders.
click here to find a list of Ethchlorvynol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Ethchlorvynol DMF (Drug Master File) is a document detailing the whole manufacturing process of Ethchlorvynol active pharmaceutical ingredient (API) in detail. Different forms of Ethchlorvynol DMFs exist exist since differing nations have different regulations, such as Ethchlorvynol USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Ethchlorvynol DMF submitted to regulatory agencies in the US is known as a USDMF. Ethchlorvynol USDMF includes data on Ethchlorvynol's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Ethchlorvynol USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Ethchlorvynol suppliers with USDMF on PharmaCompass.
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