FDA NDC Directory · JSON-LD · Markdown

Sumatriptan

NDC 71921-170 · HUMAN PRESCRIPTION DRUG · SPRAY

Generic namesumatriptan
Labeler / ManufacturerFlorida Pharmaceutical Products, LLC.
Marketing categoryAbbreviated NDA (generic) · App ANDA208967
Dosage form / routeSPRAY · NASAL
Active ingredientsSUMATRIPTAN (20 mg/1)
Marketing started20210515
Package count1

External sources

Source: openFDA. Public-domain (CC0).