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CYCLOBENZAPRINE HYDROCHLORIDE

NDC 72189-283 · DirectRx

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

72189-283-15 — 15 TABLET, FILM COATED in 1 BOTTLE (72189-283-15)

72189-283-20 — 20 TABLET, FILM COATED in 1 BOTTLE (72189-283-20)

72189-283-30 — 30 TABLET, FILM COATED in 1 BOTTLE (72189-283-30)

72189-283-60 — 60 TABLET, FILM COATED in 1 BOTTLE (72189-283-60)

72189-283-82 — 180 TABLET, FILM COATED in 1 BOTTLE (72189-283-82)

72189-283-90 — 90 TABLET, FILM COATED in 1 BOTTLE (72189-283-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71335-2696 — Cyclobenzaprine Hydrochloride, 71610-016 — Cyclobenzaprine Hydrochloride, 71610-428 — cyclobenzaprine hydrochloride, 71610-907 — Cyclobenzaprine Hydrochloride, 71610-933 — Cyclobenzaprine, 72162-1359 — cyclobenzaprine hydrochloride, 72162-1692 — Cyclobenzaprine Hydrochloride, 72189-080 — CYCLOBENZAPRINE HYDROCHLORIDE, 72189-101 — CYCLOBENZAPRINE HYDROCHLORIDE, 72189-280 — CYCLOBENZAPRINE HYDROCHLORIDE, 72189-362 — Cyclobenzaprine HCL ER, 72189-389 — Cyclobenzaprine HCL ER, 72189-545 — Cyclobenzaprine Hydrochloride, 72189-680 — Cyclobenzaprine HCL, 72603-310 — Cyclobenzaprine Hydrochloride, 72603-311 — Cyclobenzaprine Hydrochloride, 72603-312 — Cyclobenzaprine Hydrochloride, 72789-036 — cyclobenzaprine hydrochloride, 72789-046 — cyclobenzaprine hydrochloride, 72789-073 — 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.