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CYCLOBENZAPRINE HYDROCHLORIDE

NDC 68071-4935 · NuCare Pharmaceuticals,Inc.

Generic namecyclobenzaprine hydrochloride
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

68071-4935-6 — 6 TABLET, FILM COATED in 1 BOTTLE (68071-4935-6)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 68071-4655 — cyclobenzaprine hydrochloride, 68071-4951 — cyclobenzaprine hydrochloride, 68084-753 — Cyclobenzaprine Hydrochloride, 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, +210 more

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