# Sumatriptan

NDC: 69452-346
Generic name: Sumatriptan
Labeler / Manufacturer: Bionpharma Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20220218

FDA application: ANDA078284

## 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:"69452-346"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69452-346
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e90b0eea-c424-4f00-98da-6ed6e80de1f6