# Sumatriptan

NDC: 50090-7957
Generic name: Sumatriptan
Labeler / Manufacturer: A-S Medication Solutions
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: SUBCUTANEOUS
Marketing started: 20240928

FDA application: ANDA213998

## 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:"50090-7957"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50090-7957
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7f34f450-d6f3-49a8-b55a-8e1e4a9ee950