FDA NDC Directory · JSON-LD · Markdown

GLYBURIDE

NDC 23155-057 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA090937
Dosage form / routeTABLET · ORAL
Active ingredientsGLYBURIDE (2.5 mg/1)
Marketing started20101005
Package count2

External sources

Source: openFDA. Public-domain (CC0).