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tizanidine

NDC 70771-1335 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerZydus Lifesciences Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA208187
Dosage form / routeTABLET · ORAL
Active ingredientsTIZANIDINE HYDROCHLORIDE (2 mg/1)
Marketing started20180913
Package count4

External sources

Source: openFDA. Public-domain (CC0).