# SUMATRIPTAN

NDC: 51407-673
Generic name: sumatriptan
Labeler / Manufacturer: Golden State Medical Supply, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: SUBCUTANEOUS
Marketing started: 20100610

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:"51407-673"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51407-673
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4b4915d3-be7a-e5fa-e063-6294a90a7f98