Skip to main content

CYCLOBENZAPRINE HYDROCHLORIDE

NDC 51655-539 · Northwind Health Company, LLC

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

51655-539-20 — 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-539-20)

51655-539-52 — 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-539-52)

51655-539-53 — 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-539-53)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50090-4730 — cyclobenzaprine hydrochloride, 50090-5711 — Cyclobenzaprine hydrochloride, 50090-5712 — Cyclobenzaprine hydrochloride, 50090-5713 — Cyclobenzaprine hydrochloride, 50090-5756 — Cyclobenzaprine hydrochloride, 50090-5772 — Cyclobenzaprine hydrochloride, 50090-6864 — cyclobenzaprine hydrochloride, 50268-190 — Cyclobenzaprine Hydrochloride, 50268-191 — Cyclobenzaprine, 51655-427 — cyclobenzaprine hydrochloride, 51655-592 — cyclobenzaprine hydrochloride, 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, +210 more

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