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Cyclobenzaprine Hydrochloride

NDC 70518-4692 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA218936
Dosage form / routeTABLET · ORAL
Active ingredientsCYCLOBENZAPRINE HYDROCHLORIDE (10 mg/1)
Marketing started20260707
Package count3

External sources

Source: openFDA. Public-domain (CC0).