Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
01 1Sanofi
02 1TAPI Technology & API Services
03 1Boehringer Ingelheim GmbH
04 1Curia
05 1Lek Pharmaceuticals
06 2Olon S.p.A
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 : 3169
Submission : 1978-03-06
Status :
Type : II
TAPI offers customized CDMO Solutions for API development and manufacturing services.
GDUFA
DMF Review : Complete
Rev. Date : 2013-05-31
Pay. Date : 2012-11-07
DMF Number : 14944
Submission : 2000-06-28
Status :
Type : II
A Dihydroergotamine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dihydroergotamine, including repackagers and relabelers. The FDA regulates Dihydroergotamine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dihydroergotamine 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 Dihydroergotamine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dihydroergotamine supplier is an individual or a company that provides Dihydroergotamine active pharmaceutical ingredient (API) or Dihydroergotamine finished formulations upon request. The Dihydroergotamine suppliers may include Dihydroergotamine API manufacturers, exporters, distributors and traders.
click here to find a list of Dihydroergotamine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Dihydroergotamine DMF (Drug Master File) is a document detailing the whole manufacturing process of Dihydroergotamine active pharmaceutical ingredient (API) in detail. Different forms of Dihydroergotamine DMFs exist exist since differing nations have different regulations, such as Dihydroergotamine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Dihydroergotamine DMF submitted to regulatory agencies in the US is known as a USDMF. Dihydroergotamine USDMF includes data on Dihydroergotamine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Dihydroergotamine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Dihydroergotamine suppliers with USDMF on PharmaCompass.
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