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Cyclobenzaprine Hydrochloride

NDC 60687-558 · American Health Packaging

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

60687-558-01 — 100 BLISTER PACK in 1 CARTON (60687-558-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-558-11)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 59746-211 — Cyclobenzaprine Hydrochloride, 59746-735 — Cyclobenzaprine Hydrochloride, 60429-876 — cyclobenzaprine hydrochloride, 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, 63187-157 — Cyclobenzaprine Hydrochloride, 63187-590 — Cyclobenzaprine Hydrochloride, 63187-812 — Cyclobenzaprine, +210 more

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