Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
01 1Sanofi
02 1Siegfried AG
03 1Ajinomoto OmniChem N.V.
04 1Indena
01 1DESERPIDINE
02 1DESERPIDINE AS PRODUCED IN LOUVAIN-LA-NEUVE PILOT PLANT
03 1DESERPIDINE USP
04 1RAUNORMINE
01 1Belgium
02 1France
03 1Italy
04 1Switzerland
01 4Inactive
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 : 5528
Submission : 1984-09-13
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 210
Submission : 1959-05-26
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6119
Submission : 1985-11-27
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4808
Submission : 1983-02-18
Status : Inactive
Type : II
81
PharmaCompass offers a list of Deserpidine 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 Deserpidine manufacturer or Deserpidine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Deserpidine manufacturer or Deserpidine supplier.
PharmaCompass also assists you with knowing the Deserpidine API Price utilized in the formulation of products. Deserpidine API Price is not always fixed or binding as the Deserpidine Price is obtained through a variety of data sources. The Deserpidine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A MD-0232 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MD-0232, including repackagers and relabelers. The FDA regulates MD-0232 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MD-0232 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 MD-0232 supplier is an individual or a company that provides MD-0232 active pharmaceutical ingredient (API) or MD-0232 finished formulations upon request. The MD-0232 suppliers may include MD-0232 API manufacturers, exporters, distributors and traders.
click here to find a list of MD-0232 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A MD-0232 DMF (Drug Master File) is a document detailing the whole manufacturing process of MD-0232 active pharmaceutical ingredient (API) in detail. Different forms of MD-0232 DMFs exist exist since differing nations have different regulations, such as MD-0232 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A MD-0232 DMF submitted to regulatory agencies in the US is known as a USDMF. MD-0232 USDMF includes data on MD-0232's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The MD-0232 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of MD-0232 suppliers with USDMF on PharmaCompass.
We have 4 companies offering MD-0232
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