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Ciprofloxacin

NDC 61442-224 · Carlsbad Technology, Inc.

Generic nameCiprofloxacin Hydrochloride
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)CIPROFLOXACIN HYDROCHLORIDE
Strength750 mg/1
Pharmacologic classCytochrome P450 1A2 Inhibitors [MoA], Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]
Marketing categoryANDA

Packages

61442-224-04 — 400 TABLET, FILM COATED in 1 BOTTLE (61442-224-04)

61442-224-50 — 50 TABLET, FILM COATED in 1 BOTTLE (61442-224-50)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

59651-978 — Ciprofloxacin Hydrochloride, 60429-042 — Ciprofloxacin, 60687-860 — Ciprofloxacin Hydrochloride, 60687-947 — Ciprofloxacin Hydrochloride, 60760-676 — Ciprofloxacin, 60760-689 — Ciprofolxacin, 60760-690 — Ciprofloxacin, 61314-656 — Ciprofloxacin Hydrochloride, 61442-222 — Ciprofloxacin Hydrochloride, 61442-223 — Ciprofloxacin Hydrochloride, 62135-308 — Ciprofloxacin hydrochloride, 62135-309 — Ciprofloxacin hydrochloride, 62135-310 — Ciprofloxacin hydrochloride, 62756-427 — Ciprofloxacin and dexamethasone, 63187-017 — ciprofloxacin, 63187-142 — ciprofloxacin, 63187-985 — Ciprofloxacin Hydrochloride, 63187-990 — ciprofloxacin, 63629-1010 — Ciprofloxacin Hydrochloride, 63629-3868 — Ciprofloxacin, +195 more

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