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Cyclobenzaprine Hydrochloride

NDC 59746-211 · Jubilant Cadista Pharmaceuticals Inc.

Generic nameCyclobenzaprine Hydrochloride
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

59746-211-06 — 100 TABLET, FILM COATED in 1 BOTTLE (59746-211-06)

59746-211-10 — 1000 TABLET, FILM COATED in 1 BOTTLE (59746-211-10)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

51655-818 — cyclobenzaprine hydrochloride, 51655-973 — Cyclobenzaprine, 52817-330 — cyclobenzaprine hydrochloride, 52817-331 — cyclobenzaprine hydrochloride, 52817-332 — cyclobenzaprine hydrochloride, 53746-540 — CYCLOBENZAPRINE HYDROCHLORIDE, 53746-541 — CYCLOBENZAPRINE HYDROCHLORIDE, 55154-0190 — Cyclobenzaprine Hydrochloride, 55700-239 — Cyclobenzaprine Hydrochloride, 59746-177 — Cyclobenzaprine Hydrochloride, 59746-735 — Cyclobenzaprine Hydrochloride, 60429-876 — cyclobenzaprine hydrochloride, 60687-558 — Cyclobenzaprine, 60760-766 — cyclobenzaprine hydrochloride, 60760-767 — cyclobenzaprine hydrochloride, 60760-780 — Cyclobenzaprine hydrochloride, 62332-646 — CYCLOBENZAPRINE HYDROCHLORIDE, 62332-647 — CYCLOBENZAPRINE HYDROCHLORIDE, 62332-649 — CYCLOBENZAPRINE HYDROCHLORIDE, 63187-094 — 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.