FDA NDC Directory · JSON-LD · Markdown

Tizanidine

NDC 43063-868 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerPD-Rx Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA091283
Dosage form / routeTABLET · ORAL
Active ingredientsTIZANIDINE HYDROCHLORIDE (2 mg/1)
Marketing started20130401
Package count3

External sources

Source: openFDA. Public-domain (CC0).