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Sumatriptan and Naproxen Sodium

NDC 65862-928 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA207457
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsNAPROXEN SODIUM (500 mg/1)
SUMATRIPTAN SUCCINATE (85 mg/1)
Marketing started20180215
Package count1

External sources

Source: openFDA. Public-domain (CC0).