# Sumatriptan

NDC: 71921-170
Generic name: sumatriptan
Labeler / Manufacturer: Florida Pharmaceutical Products, LLC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SPRAY
Routes: NASAL
Marketing started: 20210515

FDA application: ANDA208967

## Active ingredients

- SUMATRIPTAN: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71921-170"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71921-170
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=267dadc1-6960-4d8b-88ef-86be9c5f7159