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Cyclobenzaprine Hydrochloride

NDC 72162-1358 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namecyclobenzaprine hydrochloride
Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA077797
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCYCLOBENZAPRINE HYDROCHLORIDE (5 mg/1)
Marketing started20170330
Package count2

External sources

Source: openFDA. Public-domain (CC0).