FDA NDC Directory · JSON-LD · Markdown

Sumatriptan

NDC 69097-644 · HUMAN PRESCRIPTION DRUG · SPRAY

Labeler / ManufacturerCipla USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA214209
Dosage form / routeSPRAY · NASAL
Active ingredientsSUMATRIPTAN (20 mg/1)
Marketing started20210222
Package count1

External sources

Source: openFDA. Public-domain (CC0).