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Cyclobenzaprine Hydrochloride

NDC 71205-858 · Proficient Rx LP

Generic nameCyclobenzaprine Hydrochloride
Dosage formCAPSULE, EXTENDED RELEASE
RouteORAL
Active ingredient(s)CYCLOBENZAPRINE HYDROCHLORIDE
Strength30 mg/1
Pharmacologic classCentrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
Marketing categoryANDA

Packages

71205-858-00 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71205-858-00)

71205-858-11 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71205-858-11)

71205-858-30 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71205-858-30)

71205-858-55 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71205-858-55)

71205-858-60 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71205-858-60)

71205-858-72 120 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71205-858-72)

71205-858-90 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71205-858-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70518-4265 — Cyclobenzaprine hydrochloride, 70518-4523 — Cyclobenzaprine Hydrochloride, 70518-4692 — Cyclobenzaprine Hydrochloride, 70792-102 — Cyclobenzaprine Hydrochloride, 71205-065 — cyclobenzaprine hydrochloride, 71205-201 — cyclobenzaprine hydrochloride, 71205-356 — cyclobenzaprine hydrochloride, 71205-454 — Cyclobenzaprine Hydrochloride, 71205-678 — Cyclobenzaprine Hydrochloride, 71205-857 — Cyclobenzaprine Hydrochloride, 71335-0096 — Cyclobenzaprine Hydrochloride, 71335-1099 — cyclobenzaprine hydrochloride, 71335-1266 — cyclobenzaprine hydrochloride, 71335-1961 — Cyclobenzaprine hydrochloride, 71335-1962 — Cyclobenzaprine hydrochloride, 71335-2110 — Cyclobenzaprine Hydrochloride, 71335-2156 — Cyclobenzaprine Hydrochloride, 71335-2479 — cyclobenzaprine hydrochloride, 71335-2492 — cyclobenzaprine hydrochloride, 71335-2514 — 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.