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Triazolam

NDC 82804-275 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA214219
Dosage form / routeTABLET · ORAL
Active ingredientsTRIAZOLAM (.25 mg/1)
Marketing started20201020
Package count1

External sources

Source: openFDA. Public-domain (CC0).