# Sumatriptan Succinate

NDC: 43598-768
Generic name: Sumatriptan Succinate
Labeler / Manufacturer: Dr. Reddys Laboratories Inc.,
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: SUBCUTANEOUS
Marketing started: 20230420

FDA application: ANDA090495

## 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:"43598-768"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43598-768
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8fef1176-7a38-eca3-22ca-83efe5ca6620