01 1Bayer AG
02 1Sichuan Renan Pharmaceutical
01 1EOB-DTPA
02 1GADOXETATE DISODIUM
01 1China
02 1Germany
01 2Active
01 2Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 20414
Submission : 2007-05-14
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 39660
Submission : 2024-04-01
Status : Active
Type : II
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PharmaCompass offers a list of Gadolinium Ethoxybenzyl Dtpa API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Gadolinium Ethoxybenzyl Dtpa manufacturer or Gadolinium Ethoxybenzyl Dtpa supplier for your needs.
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PharmaCompass also assists you with knowing the Gadolinium Ethoxybenzyl Dtpa API Price utilized in the formulation of products. Gadolinium Ethoxybenzyl Dtpa API Price is not always fixed or binding as the Gadolinium Ethoxybenzyl Dtpa Price is obtained through a variety of data sources. The Gadolinium Ethoxybenzyl Dtpa Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A eovist manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of eovist, including repackagers and relabelers. The FDA regulates eovist manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. eovist API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A eovist supplier is an individual or a company that provides eovist active pharmaceutical ingredient (API) or eovist finished formulations upon request. The eovist suppliers may include eovist API manufacturers, exporters, distributors and traders.
click here to find a list of eovist suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A eovist DMF (Drug Master File) is a document detailing the whole manufacturing process of eovist active pharmaceutical ingredient (API) in detail. Different forms of eovist DMFs exist exist since differing nations have different regulations, such as eovist USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A eovist DMF submitted to regulatory agencies in the US is known as a USDMF. eovist USDMF includes data on eovist's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The eovist USDMF is kept confidential to protect the manufacturer’s intellectual property.
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