Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
01 2Sanofi
02 1Moehs Iberica
03 1ACIC Europe API & Pharmaceuticals
04 1Assia Chemical Industries Ltd
05 1Corden Pharma Bergamo S.p.A
06 1Dipharma
07 1F.I.S. Fabbrica Italiana Sintetici
08 1Ipca Laboratories
09 1Lonza Group
10 1Plantex Ltd.
11 1Siegfried AG
12 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 : 3787
Submission : 1980-04-15
Status :
Type : II
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
GDUFA
DMF Review : Complete
Rev. Date : 2013-11-20
Pay. Date : 2013-10-29
DMF Number : 6603
Submission : 1986-09-22
Status :
Type : II
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 : 4677
Submission : 1982-09-30
Status :
Type : II
52
PharmaCompass offers a list of Triamterene 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 Triamterene manufacturer or Triamterene supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Triamterene manufacturer or Triamterene supplier.
PharmaCompass also assists you with knowing the Triamterene API Price utilized in the formulation of products. Triamterene API Price is not always fixed or binding as the Triamterene Price is obtained through a variety of data sources. The Triamterene Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Dyrenium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dyrenium, including repackagers and relabelers. The FDA regulates Dyrenium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dyrenium 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 Dyrenium supplier is an individual or a company that provides Dyrenium active pharmaceutical ingredient (API) or Dyrenium finished formulations upon request. The Dyrenium suppliers may include Dyrenium API manufacturers, exporters, distributors and traders.
click here to find a list of Dyrenium suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Dyrenium DMF (Drug Master File) is a document detailing the whole manufacturing process of Dyrenium active pharmaceutical ingredient (API) in detail. Different forms of Dyrenium DMFs exist exist since differing nations have different regulations, such as Dyrenium USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Dyrenium DMF submitted to regulatory agencies in the US is known as a USDMF. Dyrenium USDMF includes data on Dyrenium's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Dyrenium USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Dyrenium suppliers with USDMF on PharmaCompass.
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