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Cyclobenzaprine Hydrochloride

NDC 50268-190 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAvPAK
Marketing categoryAbbreviated NDA (generic) · App ANDA090478
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCYCLOBENZAPRINE HYDROCHLORIDE (5 mg/1)
Marketing started20140610
Package count1

External sources

Source: openFDA. Public-domain (CC0).