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TIZANIDINE HYDROCHLORIDE

NDC 50742-225 · HUMAN PRESCRIPTION DRUG · CAPSULE

Generic nametizanidine hydrochloride
Labeler / ManufacturerIngenus Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA210267
Dosage form / routeCAPSULE · ORAL
Active ingredientsTIZANIDINE HYDROCHLORIDE (4 mg/1)
Marketing started20190320
Package count1

External sources

Source: openFDA. Public-domain (CC0).