# Sumatriptan

NDC: 68788-8535
Generic name: Sumatriptan
Labeler / Manufacturer: Preferred Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20231023

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:"68788-8535"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68788-8535
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ff08b9ee-03bf-4f5b-930e-233a3b8866af