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ciprofloxacin

NDC 68071-4679 · NuCare Pharmaceuticals,Inc.

Generic nameCiprofloxacin
Dosage formSOLUTION
RouteOPHTHALMIC
Active ingredient(s)CIPROFLOXACIN HYDROCHLORIDE
Strength3 mg/mL
Pharmacologic classCytochrome P450 1A2 Inhibitors [MoA], Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]
Marketing categoryANDA

Packages

68071-4679-5 — 5 mL in 1 BOTTLE (68071-4679-5)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68071-3699 — Ciprofolxacin, 68071-3737 — 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, 68788-4177 — Ciprofloxacin Hydrochloride, 68788-7500 — Ciprofloxacin, 68788-8136 — Ciprofloxacin Hydrochloride, 68788-8198 — Ciprofloxacin Hydrochloride, 68788-8200 — Ciprofloxacin, 68788-8692 — Ciprofolxacin, 68788-8875 — Ciprofolxacin, 69117-0008 — Ciprofloxacin Tablets, 69117-0009 — Ciprofloxacin Tablets, 69238-2432 — 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.