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Cyclobenzaprine Hydrochloride

NDC 68071-2659 · 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

68071-2659-3 — 30 TABLET, FILM COATED in 1 BOTTLE (68071-2659-3)

68071-2659-5 — 15 TABLET, FILM COATED in 1 BOTTLE (68071-2659-5)

68071-2659-6 — 6 TABLET, FILM COATED in 1 BOTTLE (68071-2659-6)

68071-2659-7 — 14 TABLET, FILM COATED in 1 BOTTLE (68071-2659-7)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

65862-190 — Cyclobenzaprine Hydrochloride, 65862-191 — Cyclobenzaprine Hydrochloride, 67046-1110 — cyclobenzaprine hydrochloride, 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, 68071-2790 — Cyclobenzaprine Hydrochloride, 68071-3150 — Cyclobenzaprine, 68071-3154 — 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, +210 more

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