FDA NDC Directory · JSON-LD · Markdown

Tetrabenazine

NDC 23155-938 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA213316
Dosage form / routeTABLET · ORAL
Active ingredientsTETRABENAZINE (12.5 mg/1)
Marketing started20250901
Package count1

External sources

Source: openFDA. Public-domain (CC0).