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Cyclobenzaprine Hydrochloride

NDC 70518-4692 · REMEDYREPACK INC.

Generic nameCyclobenzaprine Hydrochloride
Dosage formTABLET
RouteORAL
Active ingredient(s)CYCLOBENZAPRINE HYDROCHLORIDE
Strength10 mg/1
Pharmacologic classCentrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
Marketing categoryANDA

Packages

70518-4692-0 — 30 TABLET in 1 BOTTLE, PLASTIC (70518-4692-0)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70518-3415 — cyclobenzaprine hydrochloride, 70518-3474 — Cyclobenzaprine Hydrochloride, 70518-3702 — Cyclobenzaprine hydrochloride, 70518-3764 — Cyclobenzaprine Hydrochloride, 70518-3814 — cyclobenzaprine hydrochloride, 70518-4174 — Cyclobenzaprine Hydrochloride, 70518-4225 — Cyclobenzaprine Hydrochloride, 70518-4246 — Cyclobenzaprine Hydrochloride, 70518-4265 — Cyclobenzaprine hydrochloride, 70518-4523 — Cyclobenzaprine Hydrochloride, 70792-102 — Cyclobenzaprine Hydrochloride, 71205-065 — cyclobenzaprine hydrochloride, 71205-201 — cyclobenzaprine hydrochloride, 71205-356 — cyclobenzaprine hydrochloride, 71205-454 — Cyclobenzaprine Hydrochloride, 71205-678 — Cyclobenzaprine Hydrochloride, 71205-857 — Cyclobenzaprine Hydrochloride, 71205-858 — Cyclobenzaprine Hydrochloride, 71335-0096 — Cyclobenzaprine Hydrochloride, 71335-1099 — cyclobenzaprine hydrochloride, +210 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.