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Cyclobenzaprine Hydrochloride

NDC 72189-545 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerDirect_Rx
Marketing categoryAbbreviated NDA (generic) · App ANDA208170
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCYCLOBENZAPRINE HYDROCHLORIDE (10 mg/1)
Marketing started20240409
Package count5

External sources

Source: openFDA. Public-domain (CC0).