Ciprofloxacin

NDC 68071-2383 · NuCare Pharmaceuticals,Inc.

Generic nameCiprofloxacin

Dosage formTABLET, COATED

RouteORAL

Active ingredient(s)CIPROFLOXACIN HYDROCHLORIDE

Strength250 mg/1

Pharmacologic classCytochrome P450 1A2 Inhibitors [MoA], Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]

Marketing categoryANDA

Packages

68071-2383-1 — 10 TABLET, COATED in 1 BOTTLE (68071-2383-1)

68071-2383-2 — 20 TABLET, COATED in 1 BOTTLE (68071-2383-2)

68071-2383-3 — 30 TABLET, COATED in 1 BOTTLE (68071-2383-3)

68071-2383-4 — 14 TABLET, COATED in 1 BOTTLE (68071-2383-4)

68071-2383-8 — 28 TABLET, COATED in 1 BOTTLE (68071-2383-8)

68071-2383-9 — 90 TABLET, COATED in 1 BOTTLE (68071-2383-9)

FDA lists these products with the same active ingredient.

67296-1703 — Ciprofloxacin, 67296-1848 — Ciprofloxacin, 67296-1943 — Ciprofloxacin and dexamethasone, 67296-2135 — Ciprofolxacin, 67296-2169 — Ciprofolxacin, 67296-2208 — Ciprofloxacin Hydrochloride, 67296-2257 — Ciprofloxacin and Dexamethasone, 67296-2291 — Ciprofloxacin Hydrochloride, 68071-2267 — Ciprofloxacin, 68071-2269 — Ciprofloxacin, 68071-2384 — Ciprofloxacin, 68071-2404 — Ciprofloxacin, 68071-3351 — Ciprofloxacin Hydrochloride, 68071-3610 — Ciprofolxacin, 68071-3693 — Ciprofolxacin, 68071-3699 — Ciprofolxacin, 68071-3737 — Ciprofolxacin, 68071-3804 — Ciprofloxacin and Dexamethasone, 68071-3901 — Ciprofolxacin, 68071-3977 — Ciprofloxacin and dexamethasone, +195 more

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