Skip to main content

Cyclobenzaprine Hydrochloride

NDC 65862-191 · Aurobindo Pharma Limited

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

65862-191-01 — 100 TABLET, FILM COATED in 1 BOTTLE (65862-191-01)

65862-191-05 — 500 TABLET, FILM COATED in 1 BOTTLE (65862-191-05)

65862-191-99 — 1000 TABLET, FILM COATED in 1 BOTTLE (65862-191-99)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

63629-1211 — cyclobenzaprine hydrochloride, 63629-2424 — Cyclobenzaprine Hydrochloride, 63629-8206 — Cyclobenzaprine Hydrochloride, 63629-9297 — cyclobenzaprine hydrochloride, 64980-655 — Cyclobenzaprine Hydrochloride, 64980-657 — Cyclobenzaprine Hydrochloride, 64980-705 — Cyclobenzaprine Hydrochloride, 65162-540 — Cyclobenzaprine Hydrochloride, 65162-541 — Cyclobenzaprine Hydrochloride, 65862-190 — Cyclobenzaprine Hydrochloride, 67046-1110 — cyclobenzaprine hydrochloride, 67046-1566 — cyclobenzaprine hydrochloride, 67046-1645 — Cyclobenzaprine Hydrochloride, 67296-1441 — Cyclobenzaprine hydrochloride, 67296-1893 — Cyclobenzaprine Hydrochloride, 67296-2084 — cyclobenzaprine hydrochloride, 67296-2306 — Cyclobenzaprine Hydrochloride, 68071-2471 — Cyclobenzaprine hydrochloride, 68071-2659 — Cyclobenzaprine Hydrochloride, 68071-2790 — 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.