FDA NDC Directory · JSON-LD · Markdown

tizanidine hydrochloride

NDC 70710-1111 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerZydus Pharmaceuticals (USA) Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA208622
Dosage form / routeCAPSULE · ORAL
Active ingredientsTIZANIDINE HYDROCHLORIDE (2 mg/1)
Marketing started20170427
Package count3

External sources

Source: openFDA. Public-domain (CC0).