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Ciprofloxacin

NDC 72789-520 · PD-Rx Pharmaceuticals, Inc.

Generic nameCiprofloxacin Hydrochloride
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

72789-520-06 — 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-520-06)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72485-625 — Ciprofloxacin and dexamethasone, 72789-065 — Ciprofloxacin Hydrochloride, 72789-108 — Ciprofloxacin, 72789-118 — Ciprofloxacin, 72789-124 — Ciprofloxacin, 72789-125 — Ciprofloxacin, 72789-193 — Ciprofloxacin, 72789-330 — Ciprofloxacin Hydrochloride, 72789-511 — Ciprofloxacin Hydrochloride, 72789-519 — Ciprofolxacin, 72789-577 — Ciprofloxacin Hydrochloride, 72888-102 — CIPROFLOXACIN HYDROCHLORIDE, 76420-045 — Ciprofloxacin Hydrochloride, 76420-214 — Ciprofloxacin, 76420-273 — ciprofloxacin hydrochloride and hydrocortisone, 76420-588 — Ciprofloxacin, 76420-928 — Ciprofolxacin, 76420-929 — Ciprofolxacin, 76420-942 — Ciprofloxacin Hydrochloride, 80425-0192 — Ciprofloxacin HCL, +195 more

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