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CYCLOBENZAPRINE HYDROCHLORIDE

NDC 85534-0005 · HAWAII REPACK, 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

85534-0005-0 — 30 TABLET, FILM COATED in 1 BOTTLE (85534-0005-0)

85534-0005-1 — 60 TABLET, FILM COATED in 1 BOTTLE (85534-0005-1)

85534-0005-2 — 90 TABLET, FILM COATED in 1 BOTTLE (85534-0005-2)

85534-0005-3 — 120 TABLET, FILM COATED in 1 BOTTLE (85534-0005-3)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

80425-0155 — Cyclobenzaprine HCL, 80425-0292 — Cyclobenzaprine HCL, 80425-0451 — Cyclobenzaprine Hydrochloride, 80425-0460 — Cyclobenzaprine Hydrochloride, 80425-0498 — cyclobenzaprine hydrochloride, 80425-0547 — Cyclobenzaprine Hydrochloride, 82461-714 — cyclobenzaprine hydrochloride, 82461-716 — cyclobenzaprine hydrochloride, 82804-259 — cyclobenzaprine hydrochloride, 82868-008 — Cyclobenzaprine Hydrochloride, 85509-1001 — Cyclobenzaprine HCL, 85509-1014 — cyclobenzaprine hydrochloride, 85509-1035 — Cyclobenzaprine Hydrochloride, 85509-1415 — Cyclobenzaprine hydrochloride, 85509-1920 — Cyclobenzaprine Hydrochloride, 85534-0085 — cyclobenzaprine hydrochloride, 85534-0086 — cyclobenzaprine hydrochloride, 85766-003 — cyclobenzaprine hydrochloride, 85766-041 — cyclobenzaprine hydrochloride, 87441-010 — 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.