FDA NDC Directory · JSON-LD · Markdown

CYCLOBENZAPRINE HYDROCHLORIDE

NDC 72189-101 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE

Labeler / ManufacturerDIRECT RX
Marketing categoryAbbreviated NDA (generic) · App ANDA091281
Dosage form / routeCAPSULE, EXTENDED RELEASE · ORAL
Active ingredientsCYCLOBENZAPRINE HYDROCHLORIDE (15 mg/1)
Marketing started20200507
Package count1

External sources

Source: openFDA. Public-domain (CC0).