Skip to main content

Cyclobenzaprine Hydrochloride

NDC 71335-0096 · Bryant Ranch Prepack

Generic nameCyclobenzaprine Hydrochloride
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)CYCLOBENZAPRINE HYDROCHLORIDE
Strength7.5 mg/1
Pharmacologic classCentrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
Marketing categoryANDA

Packages

71335-0096-0 10 TABLET, FILM COATED in 1 BOTTLE (71335-0096-0)

71335-0096-1 60 TABLET, FILM COATED in 1 BOTTLE (71335-0096-1)

71335-0096-2 30 TABLET, FILM COATED in 1 BOTTLE (71335-0096-2)

71335-0096-3 90 TABLET, FILM COATED in 1 BOTTLE (71335-0096-3)

71335-0096-4 120 TABLET, FILM COATED in 1 BOTTLE (71335-0096-4)

71335-0096-5 15 TABLET, FILM COATED in 1 BOTTLE (71335-0096-5)

71335-0096-6 45 TABLET, FILM COATED in 1 BOTTLE (71335-0096-6)

71335-0096-7 9 TABLET, FILM COATED in 1 BOTTLE (71335-0096-7)

71335-0096-8 180 TABLET, FILM COATED in 1 BOTTLE (71335-0096-8)

71335-0096-9 14 TABLET, FILM COATED in 1 BOTTLE (71335-0096-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 71205-858 — 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, 71335-2666 — 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.