FDA NDC Directory · JSON-LD · Markdown

DIAZEPAM

NDC 11534-203 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namediazepam
Labeler / ManufacturerSunrise Pharmaceutical, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA070464
Dosage form / routeTABLET · ORAL
Active ingredientsDIAZEPAM (5 mg/1)
Marketing started20241209
Package count3

External sources

Source: openFDA. Public-domain (CC0).