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Zolpidem tartrate sublingual

NDC 49884-899 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerPar Health USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA204229
Dosage form / routeTABLET · SUBLINGUAL
Active ingredientsZOLPIDEM TARTRATE (3.5 mg/1)
Marketing started20170911
Package count1

External sources

Source: openFDA. Public-domain (CC0).