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Cyclobenzaprine Hydrochloride

NDC 76282-283 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameCyclobenzaprine
Labeler / ManufacturerEXELAN PHARMACEUTICALS, INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA090478
Dosage form / routeTABLET · ORAL
Active ingredientsCYCLOBENZAPRINE HYDROCHLORIDE (10 mg/1)
Marketing started20250410
Package count6

External sources

Source: openFDA. Public-domain (CC0).