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Ciprofloxacin Hydrochloride

NDC 68071-4235 · NuCare Pharmaceuticals,Inc.

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

Packages

68071-4235-3 — 2.5 mL in 1 BOX (68071-4235-3)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 68071-4122 — ciprofloxacin, 68071-4139 — Ciprofloxacin Hydrochloride, 68071-4260 — ciprofloxacin, 68071-4672 — Ciprofloxacin, 68071-4679 — 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, +195 more

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