# Sumatriptan

NDC: 63304-099
Generic name: Sumatriptan
Labeler / Manufacturer: SUN PHARMACEUTICAL INDUSTRIES, INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20090210

FDA application: ANDA076572

## Active ingredients

- SUMATRIPTAN SUCCINATE: 100 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63304-099"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63304-099
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c87cf537-9f7f-400e-ac4b-86e6f7e78775