# Sumatriptan

NDC: 55700-936
Generic name: Sumatriptan Succinate
Labeler / Manufacturer: Quality Care Products, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20210903
Marketing ended: 20260930
FDA application: ANDA078327

## Active ingredients

- SUMATRIPTAN SUCCINATE: 50 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"55700-936"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55700-936
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=da77dfc4-551c-4e0e-a65e-cb478f193cd9