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Serving leading biopharmaceutical companies globally:

Mallinckrodt
Chinese Patent Office
Fuji
Cantor Fitzgerald
Colorcon
Queensland Health
Farmers Insurance
US Department of Justice
Daiichi Sankyo
Johnson and Johnson

Generated: January 21, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 070261

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NDA 070261 describes METHYLDOPA, which is a drug marketed by Accord Hlthcare, Duramed Pharms Barr, Halsey, Ivax Sub Teva Pharms, Mylan, Par Pharm, Parke Davis, Pliva, Purepac Pharm, Roxane, Sandoz, Sun Pharm Industries, Superpharm, Teva, Watson Labs, Dava Pharms Inc, Abraxis Pharm, Baxter Hlthcare, Hospira, Luitpold, Marsam Pharms Llc, Smith And Nephew, and Teva Parenteral, and is included in ninety-nine NDAs. It is available from ten suppliers. Additional details are available on the METHYLDOPA profile page.

The generic ingredient in METHYLDOPA is methyldopate hydrochloride. There are three drug master file entries for this compound. One supplier is listed for this compound. Additional details are available on the methyldopate hydrochloride profile page.
Summary for 070261
Tradename:METHYLDOPA
Applicant:Watson Labs
Ingredient:methyldopa
Patents:0
Therapeutic Class:Cardiovascular Agents
Formulation / Manufacturing:see details
Medical Subject Heading (MeSH) Categories for 070261

Profile for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:TABLET;ORALStrength250MG
Approval Date:Jun 24, 1985TE:RLD:No

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Serving leading biopharmaceutical companies globally:

Colorcon
UBS
Moodys
Boehringer Ingelheim
Baxter
Daiichi Sankyo
Merck
Queensland Health
Fuji

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