Generated: August 22, 2017
DrugPatentWatch Database Preview
Details for New Drug Application (NDA): 077332
describes SUMATRIPTAN SUCCINATE
, which is a drug marketed by Teva Pharms Usa, Injectalia, Sagent Strides, Teva Parenteral, Antares Pharma Inc, Mylan Labs Ltd, West-ward Pharms Int, Aurobindo Pharma, Par Pharm, Watson Labs, Fresenius Kabi Usa, Teva, Sagent Agila, Roxane, Mylan, Dr Reddys Labs Inc, Sun Pharm Inds Ltd, Aurobindo Pharma Ltd, Sun Pharma Global, Apotex Inc, Sandoz Inc, Par Sterile Products, Sandoz, Hikma Farmaceutica, Orchid Hlthcare, Wockhardt, Sun Pharm Inds, and Hikma Pharms, and is included in thirty-two NDAs. It is available from thirty-seven suppliers. Additional details are available on the SUMATRIPTAN SUCCINATE profile page.
The generic ingredient in SUMATRIPTAN SUCCINATE is sumatriptan succinate. There are twenty-three drug master file entries for this compound. Forty-seven suppliers are listed for this compound. Additional details are available on the sumatriptan succinate profile page.
Summary for NDA: 077332
|Formulation / Manufacturing:||see details|Complete Access Available with Subscription
Summary for product number 001
|Active Rx/OTC/Discontinued:||RX||Dosage:||INJECTABLE;SUBCUTANEOUS||Strength||EQ 6MG BASE/0.5ML (EQ 12MG BASE/ML)|
|Approval Date:||Oct 9, 2009||TE:||AP||RLD:||No|
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