Last Updated: November 13, 2026

Details for New Drug Application (NDA): 077907

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NDA 077907 describes SUMATRIPTAN SUCCINATE, which is a drug marketed by Baxter Hlthcare Corp, Caplin, Eugia Pharma, Fresenius Kabi Usa, Hikma, Onesource Specialty, Ph Health, Pharmobedient, Sandoz, Teva Parenteral, Teva Pharms Usa, Wockhardt Bio Ag, Zydus, Aurobindo Pharma, Dr Reddys Labs Inc, Fosun Pharma, Hikma Pharms, Ipca Labs Ltd, Mylan, Orbion Pharms, Roxane, Sun Pharm Inds, Sun Pharm Inds Ltd, Teva, Vkt Pharma, Watson Labs, Zhejiang, Alembic, Antares Pharma Inc, Dr Reddys, and Sun Pharm, and is included in thirty-eight NDAs. It is available from thirty-one suppliers. Additional details are available on the SUMATRIPTAN SUCCINATE profile page.

The generic ingredient in SUMATRIPTAN SUCCINATE is sumatriptan succinate. There is one drug master file entry for this compound. Thirty-six suppliers are listed for this compound. Additional details are available on the sumatriptan succinate profile page.

Summary for 077907

Tradename:	SUMATRIPTAN SUCCINATE
Applicant:	Teva Pharms Usa
Ingredient:	sumatriptan succinate
Patents:	0

Profile for product number 001

Active Rx/OTC/Discontinued:	DISCN	Dosage:	SOLUTION;SUBCUTANEOUS			Strength	EQ 6MG BASE/0.5ML (EQ 12MG BASE/ML)
Approval Date:	Feb 6, 2009	TE:		RLD:	No

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