FDA NDC Directory · JSON-LD · Markdown

Selegiline Hydrochloride

NDC 72319-006 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / Manufactureri3 Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA074672
Dosage form / routeTABLET · ORAL
Active ingredientsSELEGILINE HYDROCHLORIDE (5 mg/1)
Marketing started20211215
Package count1

External sources

Source: openFDA. Public-domain (CC0).