01 1The Dow Chemical Company
01 1VERSENE NA CHELATING AGENT
01 1U.S.A
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 11287
Submission : 1994-12-29
Status : Inactive
Type : II
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PharmaCompass offers a list of Edetate Sodium API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Edetate Sodium manufacturer or Edetate Sodium supplier for your needs.
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A Ergon manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ergon, including repackagers and relabelers. The FDA regulates Ergon manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ergon 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 Ergon supplier is an individual or a company that provides Ergon active pharmaceutical ingredient (API) or Ergon finished formulations upon request. The Ergon suppliers may include Ergon API manufacturers, exporters, distributors and traders.
click here to find a list of Ergon suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Ergon DMF (Drug Master File) is a document detailing the whole manufacturing process of Ergon active pharmaceutical ingredient (API) in detail. Different forms of Ergon DMFs exist exist since differing nations have different regulations, such as Ergon USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Ergon DMF submitted to regulatory agencies in the US is known as a USDMF. Ergon USDMF includes data on Ergon's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Ergon USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Ergon suppliers with USDMF on PharmaCompass.
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