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Cyclobenzaprine Hydrochloride

NDC 76420-271 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAsclemed USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA071611
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCYCLOBENZAPRINE HYDROCHLORIDE (10 mg/1)
Marketing started20210720
Package count10

External sources

Source: openFDA. Public-domain (CC0).