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Cyclobenzaprine Hydrochloride

NDC 68071-2659 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerNuCare Pharmaceuticals,Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA078643
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCYCLOBENZAPRINE HYDROCHLORIDE (10 mg/1)
Marketing started20080926
Package count4

External sources

Source: openFDA. Public-domain (CC0).