Cyclobenzaprine Hydrochloride

NDC 68071-3154 · NuCare Pharmaceuticals, Inc.

Generic nameCyclobenzaprine

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)CYCLOBENZAPRINE HYDROCHLORIDE

Strength10 mg/1

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

Marketing categoryANDA

Packages

68071-3154-1 — 10 TABLET, FILM COATED in 1 BOTTLE (68071-3154-1)

68071-3154-3 — 30 TABLET, FILM COATED in 1 BOTTLE (68071-3154-3)

68071-3154-6 — 6 TABLET, FILM COATED in 1 BOTTLE (68071-3154-6)

68071-3154-7 — 7 TABLET, FILM COATED in 1 BOTTLE (68071-3154-7)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

67046-1566 — cyclobenzaprine hydrochloride, 67046-1645 — Cyclobenzaprine Hydrochloride, 67296-1441 — Cyclobenzaprine hydrochloride, 67296-1893 — Cyclobenzaprine Hydrochloride, 67296-2084 — cyclobenzaprine hydrochloride, 67296-2306 — Cyclobenzaprine Hydrochloride, 68071-2471 — Cyclobenzaprine hydrochloride, 68071-2659 — Cyclobenzaprine Hydrochloride, 68071-2790 — Cyclobenzaprine Hydrochloride, 68071-3150 — Cyclobenzaprine, 68071-3404 — Cyclobenzaprine Hydrochloride, 68071-3462 — cyclobenzaprine hydrochloride, 68071-3475 — cyclobenzaprine hydrochloride, 68071-3561 — cyclobenzaprine hydrochloride, 68071-3567 — Cyclobenzaprine hydrochloride, 68071-3627 — Cyclobenzaprine Hydrochloride, 68071-3805 — Cyclobenzaprine Hydrochloride, 68071-3915 — Cyclobenzaprine Hydrochloride, 68071-3973 — Cyclobenzaprine Hydrochloride, 68071-3981 — Cyclobenzaprine Hydrochloride, +210 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.