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Zolpidem Tartrate

NDC 80425-0513 · HUMAN PRESCRIPTION DRUG · TABLET, COATED

Labeler / ManufacturerAdvanced Rx of Tennessee, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA077322
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsZOLPIDEM TARTRATE (5 mg/1)
Marketing started20250415
Package count3

External sources

Source: openFDA. Public-domain (CC0).