# Sumatriptan

NDC: 69097-644
Generic name: Sumatriptan
Labeler / Manufacturer: Cipla USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SPRAY
Routes: NASAL
Marketing started: 20210222

FDA application: ANDA214209

## 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:"69097-644"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69097-644
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=559cca31-c0d2-45bf-999d-e92fc49a4a89