FDA NDC Directory · JSON-LD · Markdown

Tizanidine

NDC 72789-327 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerPD-Rx Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA076416
Dosage form / routeTABLET · ORAL
Active ingredientsTIZANIDINE HYDROCHLORIDE (4 mg/1)
Marketing started20031211
Package count1

External sources

Source: openFDA. Public-domain (CC0).