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Cyclobenzaprine Hydrochloride

NDC 64980-655 · Rising Pharma Holdings, Inc.

Generic nameCyclobenzaprine Hydrochloride
Dosage formTABLET
RouteORAL
Active ingredient(s)CYCLOBENZAPRINE HYDROCHLORIDE
Strength5 mg/1
Pharmacologic classCentrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
Marketing categoryANDA

Packages

64980-655-01 — 100 TABLET in 1 BOTTLE (64980-655-01)

64980-655-10 — 1000 TABLET in 1 BOTTLE (64980-655-10)

64980-655-50 — 500 TABLET in 1 BOTTLE (64980-655-50)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

63187-157 — Cyclobenzaprine Hydrochloride, 63187-590 — Cyclobenzaprine Hydrochloride, 63187-812 — Cyclobenzaprine, 63459-700 — Cyclobenzaprine Hydrochloride, 63459-701 — Cyclobenzaprine Hydrochloride, 63629-1210 — cyclobenzaprine hydrochloride, 63629-1211 — cyclobenzaprine hydrochloride, 63629-2424 — Cyclobenzaprine Hydrochloride, 63629-8206 — Cyclobenzaprine Hydrochloride, 63629-9297 — cyclobenzaprine hydrochloride, 64980-657 — Cyclobenzaprine Hydrochloride, 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, +210 more

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