FDA NDC Directory · JSON-LD · Markdown

Sumatriptan

NDC 70069-804 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerSomerset Therapeutics, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA213998
Dosage form / routeINJECTION, SOLUTION · SUBCUTANEOUS
Active ingredientsSUMATRIPTAN SUCCINATE (6 mg/.5mL)
Marketing started20211025
Package count2

External sources

Source: openFDA. Public-domain (CC0).