Sumatriptan Succinate

Product NDC

0703-7351

11-digit product format

007037351

Labeler code

0703

Product ID

0703-7351_cd4aef29-53e1-4dce-9eee-09bcf6e4e24c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Sumatriptan Succinate

Dosage form

INJECTION, SOLUTION

Route

SUBCUTANEOUS

Labeler

Teva Parenteral Medicines, Inc.

Application

ANDA077907

Marketing category

ANDA

Marketing start

2009-02-06

Marketing end

0000-00-00

Substance

SUMATRIPTAN SUCCINATE

Active strength

6 mg/.5mL

Pharmacologic classes

Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC],Serotonin 1b Receptor Agonists [MoA]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record