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ZOLPIDEM TARTRATE

NDC 71610-904 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namezolpidem tartrate
Labeler / ManufacturerAphena Pharma Solutions - Tennessee, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA077214
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsZOLPIDEM TARTRATE (5 mg/1)
Marketing started20070423
Package count9

External sources

Source: openFDA. Public-domain (CC0).