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Cyclobenzaprine Hydrochloride

NDC 16571-783 · Rising Pharma Holdings, Inc.

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

16571-783-01 — 100 TABLET, FILM COATED in 1 BOTTLE (16571-783-01)

16571-783-10 — 1000 TABLET, FILM COATED in 1 BOTTLE (16571-783-10)

16571-783-50 — 500 TABLET, FILM COATED in 1 BOTTLE (16571-783-50)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0093-3422 — Cyclobenzaprine Hydrochloride, 0115-1436 — Cyclobenzaprine Hydrochloride, 0115-1437 — Cyclobenzaprine Hydrochloride, 0615-8084 — Cyclobenzaprine, 0615-8508 — Cyclobenzaprine hydrochloride, 0904-7400 — Cyclobenzaprine Hydrochloride, 0904-7401 — Cyclobenzaprine Hydrochloride, 10702-006 — Cyclobenzaprine Hydrochloride, 10702-007 — Cyclobenzaprine Hydrochloride, 16571-782 — Cyclobenzaprine Hydrochloride, 24979-035 — Cyclobenzaprine Hydrochloride, 24979-036 — Cyclobenzaprine Hydrochloride, 29300-413 — Cyclobenzaprine hydrochloride, 29300-414 — Cyclobenzaprine hydrochloride, 29300-415 — Cyclobenzaprine hydrochloride, 33342-272 — Cyclobenzaprine Hydrochloride, 33342-273 — Cyclobenzaprine Hydrochloride, 42291-154 — Cyclobenzaprine Hydrochloride, 42708-172 — Cyclobenzaprine Hydrochloride, 42708-197 — 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.