FDA NDC Directory · JSON-LD · Markdown

Modafinil

NDC 23155-862 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA207196
Dosage form / routeTABLET · ORAL
Active ingredientsMODAFINIL (200 mg/1)
Marketing started20240221
Package count4

External sources

Source: openFDA. Public-domain (CC0).