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Ciprofloxacin

NDC 68071-3737 · NuCare Pharmaceutical, Inc.

Generic nameCiprofolxacin
Dosage formTABLET
RouteORAL
Active ingredient(s)CIPROFLOXACIN HYDROCHLORIDE
Strength500 mg/1
Pharmacologic classCytochrome P450 1A2 Inhibitors [MoA], Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]
Marketing categoryANDA

Packages

68071-3737-2 — 2 TABLET in 1 BOTTLE (68071-3737-2)

68071-3737-6 — 6 TABLET in 1 BOTTLE (68071-3737-6)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

67296-2291 — Ciprofloxacin Hydrochloride, 68071-2267 — Ciprofloxacin, 68071-2269 — Ciprofloxacin, 68071-2383 — Ciprofloxacin, 68071-2384 — Ciprofloxacin, 68071-2404 — Ciprofloxacin, 68071-3351 — Ciprofloxacin Hydrochloride, 68071-3610 — Ciprofolxacin, 68071-3693 — Ciprofolxacin, 68071-3699 — Ciprofolxacin, 68071-3804 — Ciprofloxacin and Dexamethasone, 68071-3901 — Ciprofolxacin, 68071-3977 — Ciprofloxacin and dexamethasone, 68071-4122 — ciprofloxacin, 68071-4139 — Ciprofloxacin Hydrochloride, 68071-4235 — Ciprofloxacin Hydrochloride, 68071-4260 — ciprofloxacin, 68071-4672 — Ciprofloxacin, 68071-4679 — Ciprofloxacin, 68788-4177 — Ciprofloxacin Hydrochloride, +195 more

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