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Cyclobenzaprine Hydrochloride

NDC 43547-400 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namecyclobenzaprine hydrochloride
Labeler / ManufacturerSolco Healthcare U.S., LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA077797
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCYCLOBENZAPRINE HYDROCHLORIDE (10 mg/1)
Marketing started20170330
Package count8

External sources

Source: openFDA. Public-domain (CC0).