FDA NDC Directory · JSON-LD · Markdown

Zolpidem Tartrate

NDC 71610-151 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAphena Pharma Solutions - Tennessee, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA078413
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsZOLPIDEM TARTRATE (5 mg/1)
Marketing started20070504
Package count7

External sources

Source: openFDA. Public-domain (CC0).