Skip to main content

Cyclobenzaprine Hydrochloride

NDC 69420-1001 · SA3, LLC

Generic nameCyclobenzaprine Hydrochloride
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)CYCLOBENZAPRINE HYDROCHLORIDE
Strength7.5 mg/1
Pharmacologic classCentrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
Marketing categoryANDA

Packages

69420-1001-1 — 1000 TABLET, FILM COATED in 1 BOTTLE (69420-1001-1)

69420-1001-2 — 100 TABLET, FILM COATED in 1 BOTTLE (69420-1001-2)

69420-1001-3 — 30 TABLET, FILM COATED in 1 BOTTLE (69420-1001-3)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68788-8471 — cyclobenzaprine hydrochloride, 68788-8474 — cyclobenzaprine hydrochloride, 68788-8522 — Cyclobenzaprine Hydrochloride, 68788-8637 — Cyclobenzaprine hydrochloride, 68788-8706 — Cyclobenzaprine hydrochloride, 68788-9967 — Cyclobenzaprine Hydrochloride, 69097-845 — Cyclobenzaprine, 69097-846 — Cyclobenzaprine, 69306-015 — Cyclobenzaprine Hydrochloride, 69306-872 — Cyclobenzaprine Hydrochloride, 70512-872 — Cyclobenzaprine Hydrochloride, 70518-2611 — cyclobenzaprine hydrochloride, 70518-3251 — Cyclobenzaprine hydrochloride, 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, +210 more

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