FDA NDC Directory · JSON-LD · Markdown

Selegiline Hydrochloride

NDC 60505-3438 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerApotex Corp.
Marketing categoryAbbreviated NDA (generic) · App ANDA074871
Dosage form / routeTABLET · ORAL
Active ingredientsSELEGILINE HYDROCHLORIDE (5 mg/1)
Marketing started19970706
Package count2

External sources

Source: openFDA. Public-domain (CC0).