# Sumatriptan Succinate

NDC: 71205-111
Generic name: Sumatriptan Succinate
Labeler / Manufacturer: Proficient Rx LP
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: SUBCUTANEOUS
Marketing started: 20090206

FDA application: ANDA078593

## 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:"71205-111"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71205-111
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=44d6d757-489c-4262-a518-af8c470734d6