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Cyclobenzaprine Hydrochloride

NDC 71610-428 · Aphena Pharma Solutions - Tennessee, 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

71610-428-45 — 45 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-428-45)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71335-2110 — Cyclobenzaprine Hydrochloride, 71335-2156 — Cyclobenzaprine Hydrochloride, 71335-2479 — cyclobenzaprine hydrochloride, 71335-2492 — cyclobenzaprine hydrochloride, 71335-2514 — Cyclobenzaprine Hydrochloride, 71335-2666 — Cyclobenzaprine Hydrochloride, 71335-2678 — Cyclobenzaprine Hydrochloride, 71335-2686 — cyclobenzaprine hydrochloride, 71335-2696 — Cyclobenzaprine Hydrochloride, 71610-016 — 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, 72189-283 — CYCLOBENZAPRINE HYDROCHLORIDE, 72189-362 — Cyclobenzaprine HCL ER, 72189-389 — Cyclobenzaprine HCL ER, +210 more

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