Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
01 1Sanofi
02 1AXYNTIS Group
03 1Gedeon Richter
04 1RHODIA INC US 08512-7500 Cranbury
01 2ETHIONAMIDE
02 1ETHIONAMIDE DRUG SUBSTANCE
03 1ETHIONAMIDE SUPPOSITORIES, 500 MG, THERAPLIX SA, PARIS, FR
01 2France
02 1Hungary
03 1U.S.A
01 1Active
02 3Inactive
01 4Blank
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 8010
Submission : 1989-04-03
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 23640
Submission : 2010-03-17
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5604
Submission : 1984-11-07
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 435
Submission : 1961-06-22
Status : Inactive
Type : II
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PharmaCompass offers a list of Ethionamide 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 Ethionamide manufacturer or Ethionamide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ethionamide manufacturer or Ethionamide supplier.
PharmaCompass also assists you with knowing the Ethionamide API Price utilized in the formulation of products. Ethionamide API Price is not always fixed or binding as the Ethionamide Price is obtained through a variety of data sources. The Ethionamide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Etionamida manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Etionamida, including repackagers and relabelers. The FDA regulates Etionamida manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Etionamida API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Etionamida manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Etionamida supplier is an individual or a company that provides Etionamida active pharmaceutical ingredient (API) or Etionamida finished formulations upon request. The Etionamida suppliers may include Etionamida API manufacturers, exporters, distributors and traders.
click here to find a list of Etionamida suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Etionamida DMF (Drug Master File) is a document detailing the whole manufacturing process of Etionamida active pharmaceutical ingredient (API) in detail. Different forms of Etionamida DMFs exist exist since differing nations have different regulations, such as Etionamida USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Etionamida DMF submitted to regulatory agencies in the US is known as a USDMF. Etionamida USDMF includes data on Etionamida's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Etionamida USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Etionamida suppliers with USDMF on PharmaCompass.
We have 4 companies offering Etionamida
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