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Ciprofloxacin

NDC 72789-118 · PD-Rx Pharmaceuticals, Inc.

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

72789-118-01 — 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-118-01)

72789-118-20 — 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-118-20)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72189-111 — ciprofloxacin hydrochloride, 72189-300 — CIPROFLOXACIN, 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, 72789-124 — Ciprofloxacin, 72789-125 — Ciprofloxacin, 72789-193 — Ciprofloxacin, 72789-330 — Ciprofloxacin Hydrochloride, 72789-511 — Ciprofloxacin Hydrochloride, 72789-519 — Ciprofolxacin, 72789-520 — Ciprofloxacin Hydrochloride, 72789-577 — Ciprofloxacin Hydrochloride, 72888-102 — CIPROFLOXACIN HYDROCHLORIDE, 76420-045 — 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.