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Cyclobenzaprine Hydrochloride

NDC 72603-310 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerNORTHSTAR RX LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA208170
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCYCLOBENZAPRINE HYDROCHLORIDE (5 mg/1)
Marketing started20170531
Package count2

External sources

Source: openFDA. Public-domain (CC0).