Cyclobenzaprine Hydrochloride

NDC 69097-845 · Cipla USA Inc.

Generic nameCyclobenzaprine

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)CYCLOBENZAPRINE HYDROCHLORIDE

Strength5 mg/1

Pharmacologic classCentrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]

Marketing categoryANDA

Packages

69097-845-07 — 100 TABLET, FILM COATED in 1 BOTTLE (69097-845-07)

69097-845-15 — 1000 TABLET, FILM COATED in 1 BOTTLE (69097-845-15)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68788-4087 — Cyclobenzaprine Hydrochloride, 68788-4154 — Cyclobenzaprine Hydrochloride, 68788-8167 — Cyclobenzaprine Hydrochloride, 68788-8221 — Cyclobenzaprine Hydrochloride, 68788-8471 — cyclobenzaprine hydrochloride, 68788-8474 — cyclobenzaprine hydrochloride, 68788-8522 — Cyclobenzaprine Hydrochloride, 68788-8637 — Cyclobenzaprine hydrochloride, 68788-8706 — Cyclobenzaprine hydrochloride, 68788-9967 — Cyclobenzaprine Hydrochloride, 69097-846 — Cyclobenzaprine, 69306-015 — Cyclobenzaprine Hydrochloride, 69306-872 — Cyclobenzaprine Hydrochloride, 69420-1001 — 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, +210 more

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