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Serving hundreds of leading biopharmaceutical companies globally:

Covington
Chubb
McKesson
Baxter
Chinese Patent Office
Fish and Richardson
Colorcon
US Department of Justice
Teva

Generated: April 23, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 203322

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NDA 203322 describes SUMATRIPTAN SUCCINATE, which is a drug marketed by Antares Pharma Inc, Aurobindo Pharma Ltd, Dr Reddys Labs Inc, Fresenius Kabi Usa, Hikma Farmaceutica, Injectalia, Mylan Asi, Mylan Labs Ltd, Par Pharm, Par Sterile Products, Sandoz Inc, Sun Pharma Global, Teva Parenteral, Teva Pharms Usa, West-ward Pharms Int, Wockhardt, Apotex Inc, Aurobindo Pharma, Fosun Pharma, Hikma Pharms, Mylan, Orchid Hlthcare, Roxane, Sun Pharm Inds, Sun Pharm Inds Ltd, Teva, and Watson Labs, and is included in thirty-two NDAs. It is available from thirty-two suppliers. Additional details are available on the SUMATRIPTAN SUCCINATE profile page.

The generic ingredient in SUMATRIPTAN SUCCINATE is sumatriptan succinate. There are twenty-four drug master file entries for this compound. Thirty-seven suppliers are listed for this compound. Additional details are available on the sumatriptan succinate profile page.
Summary for 203322
Tradename:SUMATRIPTAN SUCCINATE
Applicant:Mylan Labs Ltd
Ingredient:sumatriptan succinate
Patents:0
Formulation / Manufacturing:see details

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:INJECTABLE;SUBCUTANEOUSStrengthEQ 6MG BASE/0.5ML (EQ 12MG BASE/ML)
Approval Date:Apr 14, 2014TE:APRLD:No

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Serving hundreds of leading biopharmaceutical companies globally:

Mallinckrodt
Argus Health
Baxter
Chubb
Johnson and Johnson
Teva
Medtronic
Express Scripts
Daiichi Sankyo

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