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Alprazolam

NDC 69339-201 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerNatco Pharma USA LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA200739
Dosage form / routeTABLET · ORAL
Active ingredientsALPRAZOLAM (1 mg/1)
Marketing started20230728
Package count3

External sources

Source: openFDA. Public-domain (CC0).