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ciprofloxacin

NDC 71205-300 · Proficient Rx LP

Generic nameCiprofloxacin
Dosage formSOLUTION
RouteOPHTHALMIC
Active ingredient(s)CIPROFLOXACIN HYDROCHLORIDE
Strength3 mg/mL
Pharmacologic classQuinolone Antimicrobial [EPC], Quinolones [CS]
Marketing categoryANDA

Packages

71205-300-05 — 1 BOTTLE, PLASTIC in 1 CARTON (71205-300-05) / 5 mL in 1 BOTTLE, PLASTIC

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

69367-386 — Ciprofloxacin Hydrochloride, 69367-387 — Ciprofloxacin Hydrochloride, 70244-033 — Ciprofloxacin and dexamethasone, 70518-1170 — Ciprofloxacin Hydrochloride, 70518-2837 — Ciprofloxacin, 70518-3063 — Ciprofloxacin, 70518-4133 — Ciprofolxacin, 70518-4214 — Ciprofloxacin Hydrochloride, 70518-4229 — Ciprofolxacin, 70934-965 — Ciprofloxacin Hydrochloride, 71205-636 — Ciprofloxacin Hydrochloride, 71205-649 — Ciprofloxacin Hydrochloride, 71205-749 — Ciprofloxacin, 71205-997 — Ciprofloxacin Hydrochloride, 71335-0070 — ciprofloxacin, 71335-0408 — ciprofloxacin, 71335-1024 — Ciprofloxacin Hydrochloride, 71335-1152 — Ciprofloxacin Tablets, 71335-1229 — Ciprofloxacin Tablets, 71335-1347 — 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.