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TIZANIDINE

NDC 84386-024 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA076282
Dosage form / routeTABLET · ORAL
Active ingredientsTIZANIDINE HYDROCHLORIDE (4 mg/1)
Marketing started20260901
Package count2

External sources

Source: openFDA. Public-domain (CC0).