FDA NDC Directory · JSON-LD · Markdown

TIZANIDINE HYDROCHLORIDE

NDC 61919-196 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerTIZANIDINE HYDROCHLORIDE
Marketing categoryAbbreviated NDA (generic) · App ANDA091283
Dosage form / routeTABLET · ORAL
Active ingredientsTIZANIDINE HYDROCHLORIDE (4 mg/1)
Marketing started20140101
Package count6

External sources

Source: openFDA. Public-domain (CC0).