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Zolpidem Tartrate

NDC 51991-982 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerBreckenridge Pharmaceutical, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA213592
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsZOLPIDEM TARTRATE (12.5 mg/1)
Marketing started20260301
Package count1

External sources

Source: openFDA. Public-domain (CC0).