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CYCLOBENZAPRINE HYDROCHLORIDE

NDC 67296-2084 · Redpharm Drug

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

67296-2084-1 — 15 TABLET, FILM COATED in 1 BOTTLE (67296-2084-1)

67296-2084-2 — 10 TABLET, FILM COATED in 1 BOTTLE (67296-2084-2)

67296-2084-3 — 30 TABLET, FILM COATED in 1 BOTTLE (67296-2084-3)

67296-2084-4 — 21 TABLET, FILM COATED in 1 BOTTLE (67296-2084-4)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

64980-705 — Cyclobenzaprine Hydrochloride, 65162-540 — Cyclobenzaprine Hydrochloride, 65162-541 — Cyclobenzaprine Hydrochloride, 65862-190 — Cyclobenzaprine Hydrochloride, 65862-191 — Cyclobenzaprine Hydrochloride, 67046-1110 — cyclobenzaprine hydrochloride, 67046-1566 — cyclobenzaprine hydrochloride, 67046-1645 — Cyclobenzaprine Hydrochloride, 67296-1441 — Cyclobenzaprine hydrochloride, 67296-1893 — Cyclobenzaprine Hydrochloride, 67296-2306 — Cyclobenzaprine Hydrochloride, 68071-2471 — Cyclobenzaprine hydrochloride, 68071-2659 — Cyclobenzaprine Hydrochloride, 68071-2790 — Cyclobenzaprine Hydrochloride, 68071-3150 — Cyclobenzaprine, 68071-3154 — Cyclobenzaprine, 68071-3404 — Cyclobenzaprine Hydrochloride, 68071-3462 — cyclobenzaprine hydrochloride, 68071-3475 — cyclobenzaprine hydrochloride, 68071-3561 — 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.