FDA NDC Directory · JSON-LD · Markdown

GLYBURIDE

NDC 62135-583 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerChartwell RX, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA090937
Dosage form / routeTABLET · ORAL
Active ingredientsGLYBURIDE (1.25 mg/1)
Marketing started20101005
Package count1

External sources

Source: openFDA. Public-domain (CC0).