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Cyclobenzaprine hydrochloride

NDC 71335-1962 · Bryant Ranch Prepack

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

71335-1962-0 40 TABLET, FILM COATED in 1 BOTTLE (71335-1962-0)

71335-1962-1 14 TABLET, FILM COATED in 1 BOTTLE (71335-1962-1)

71335-1962-2 84 TABLET, FILM COATED in 1 BOTTLE (71335-1962-2)

71335-1962-3 30 TABLET, FILM COATED in 1 BOTTLE (71335-1962-3)

71335-1962-4 20 TABLET, FILM COATED in 1 BOTTLE (71335-1962-4)

71335-1962-5 15 TABLET, FILM COATED in 1 BOTTLE (71335-1962-5)

71335-1962-6 60 TABLET, FILM COATED in 1 BOTTLE (71335-1962-6)

71335-1962-7 90 TABLET, FILM COATED in 1 BOTTLE (71335-1962-7)

71335-1962-8 56 TABLET, FILM COATED in 1 BOTTLE (71335-1962-8)

71335-1962-9 120 TABLET, FILM COATED in 1 BOTTLE (71335-1962-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71205-201 — cyclobenzaprine hydrochloride, 71205-356 — cyclobenzaprine hydrochloride, 71205-454 — Cyclobenzaprine Hydrochloride, 71205-678 — Cyclobenzaprine Hydrochloride, 71205-857 — Cyclobenzaprine Hydrochloride, 71205-858 — Cyclobenzaprine Hydrochloride, 71335-0096 — Cyclobenzaprine Hydrochloride, 71335-1099 — cyclobenzaprine hydrochloride, 71335-1266 — cyclobenzaprine hydrochloride, 71335-1961 — 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, 71335-2678 — Cyclobenzaprine Hydrochloride, 71335-2686 — cyclobenzaprine hydrochloride, 71335-2696 — Cyclobenzaprine Hydrochloride, 71610-016 — 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.