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Cyclobenzaprine hydrochloride

NDC 76420-256 · Asclemed USA, Inc.

Generic nameCyclobenzaprine hydrochloride
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)CYCLOBENZAPRINE HYDROCHLORIDE
Strength7.5 mg/1
Pharmacologic classCentrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
Marketing categoryANDA

Packages

76420-256-30 — 100 TABLET, FILM COATED in 1 BOTTLE (76420-256-30)

76420-256-60 — 60 TABLET, FILM COATED in 1 BOTTLE (76420-256-60)

76420-256-90 — 90 TABLET, FILM COATED in 1 BOTTLE (76420-256-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72789-156 — cyclobenzaprine hydrochloride, 72789-547 — cyclobenzaprine hydrochloride, 72888-012 — cyclobenzaprine hydrochloride, 72888-013 — cyclobenzaprine hydrochloride, 72888-014 — cyclobenzaprine hydrochloride, 76282-283 — Cyclobenzaprine, 76420-010 — Cyclobenzaprine Hydrochloride, 76420-011 — cyclobenzaprine hydrochloride, 76420-030 — cyclobenzaprine hydrochloride, 76420-033 — cyclobenzaprine hydrochloride, 76420-265 — cyclobenzaprine hydrochloride, 76420-268 — Cyclobenzaprine Hydrochloride, 76420-269 — Cyclobenzaprine Hydrochloride, 76420-271 — Cyclobenzaprine Hydrochloride, 76420-599 — Cyclobenzaprine Hydrochloride, 76420-828 — cyclobenzaprine hydrochloride, 76420-829 — cyclobenzaprine hydrochloride, 76420-830 — cyclobenzaprine hydrochloride, 76420-839 — Cyclobenzaprine hydrochloride, 76420-840 — 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.