FDA NDC Directory · JSON-LD · Markdown

tizanidine

NDC 68788-8741 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerPreferred Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA076533
Dosage form / routeTABLET · ORAL
Active ingredientsTIZANIDINE HYDROCHLORIDE (4 mg/1)
Marketing started20240920
Package count6

External sources

Source: openFDA. Public-domain (CC0).