# sumatriptan

NDC: 83270-151
Generic name: sumatriptan
Labeler / Manufacturer: ONESOURCE SPECIALTY PHARMA LIMITED
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: SUBCUTANEOUS
Marketing started: 20260202

FDA application: ANDA090314

## Active ingredients

- SUMATRIPTAN SUCCINATE: 6 mg/.5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"83270-151"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=83270-151
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=587e6bb5-a665-4396-814e-ce893a20290b