CIPROFLOXACIN

NDC 72189-300 · DirectRx

Generic nameCIPROFLOXACIN

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)CIPROFLOXACIN HYDROCHLORIDE

Strength500 mg/1

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

Marketing categoryANDA

Packages

72189-300-06 — 6 TABLET, FILM COATED in 1 BOTTLE (72189-300-06)

72189-300-20 — 20 TABLET, FILM COATED in 1 BOTTLE (72189-300-20)

FDA lists these products with the same active ingredient.

71335-2097 — Ciprofloxacin, 71335-2450 — Ciprofolxacin, 71335-2502 — Ciprofolxacin, 71610-081 — Ciprofloxacin, 71610-109 — Ciprofloxacin Hydrochloride, 71610-159 — Ciprofloxacin Hydrochloride, 72162-1740 — Ciprofloxacin Hydrochloride, 72162-1741 — Ciprofloxacin Hydrochloride, 72162-2425 — Ciprofolxacin, 72189-111 — ciprofloxacin hydrochloride, 72189-304 — Ciprofloxacin, 72189-323 — CIPROFLOXACIN, 72189-616 — Ciprofloxacin, 72189-623 — Ciprofloxacin, 72189-627 — Ciprofloxacin, 72485-625 — Ciprofloxacin and dexamethasone, 72789-065 — Ciprofloxacin Hydrochloride, 72789-108 — Ciprofloxacin, 72789-118 — Ciprofloxacin, 72789-124 — 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.