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Cyclobenzaprine Hydrochloride

NDC 72789-073 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namecyclobenzaprine hydrochloride
Labeler / ManufacturerPD-Rx Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA077797
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCYCLOBENZAPRINE HYDROCHLORIDE (5 mg/1)
Marketing started20170330
Package count1

External sources

Source: openFDA. Public-domain (CC0).