FDA NDC Directory · JSON-LD · Markdown

Sumatriptan Succinate

NDC 63323-273 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA079242
Dosage form / routeINJECTION · SUBCUTANEOUS
Active ingredientsSUMATRIPTAN SUCCINATE (6 mg/.5mL)
Marketing started20110412
Package count1

External sources

Source: openFDA. Public-domain (CC0).