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CYCLOBENZAPRINE HYDROCHLORIDE

NDC 52817-331 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namecyclobenzaprine hydrochloride
Labeler / ManufacturerTruPharma LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA208170
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCYCLOBENZAPRINE HYDROCHLORIDE (7.5 mg/1)
Marketing started20170531
Package count1

External sources

Source: openFDA. Public-domain (CC0).