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Cyclobenzaprine Hydrochloride

NDC 85509-1920 · PHOENIX RX LLC

Generic nameCyclobenzaprine Hydrochloride
Dosage formCAPSULE, EXTENDED RELEASE
RouteORAL
Active ingredient(s)CYCLOBENZAPRINE HYDROCHLORIDE
Strength15 mg/1
Pharmacologic classCentrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
Marketing categoryNDA AUTHORIZED GENERIC

Packages

85509-1920-3 — 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (85509-1920-3)

85509-1920-6 — 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (85509-1920-6)

85509-1920-9 — 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (85509-1920-9)

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, 85534-0005 — 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.