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Cyclobenzaprine Hydrochloride

NDC 55700-239 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerQuality Care Products LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA078722
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCYCLOBENZAPRINE HYDROCHLORIDE (7.5 mg/1)
Marketing started20150325
Marketing ended20271231
Package count1

External sources

Source: openFDA. Public-domain (CC0).