# sumatriptan

NDC: 83270-005
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: 20250630

FDA application: ANDA215651

## 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:"83270-005"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=83270-005
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b4240c6e-6b9e-405f-82e6-a3d5bd9e6f29