ciprofloxacin

NDC 85293-002 · Umasuto, LLC

Generic nameciprofloxacin

Dosage formTABLET

RouteORAL

Active ingredient(s)CIPROFLOXACIN HYDROCHLORIDE

Strength250 mg/1

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

Marketing categoryANDA

Packages

85293-002-01 — 100 TABLET in 1 BOTTLE (85293-002-01)

FDA lists these products with the same active ingredient.

80425-0492 — Ciprofolxacin, 80425-0493 — Ciprofloxacin Hydrochloride, 80425-0499 — Ciprofloxacin, 82804-130 — Ciprofolxacin, 82804-256 — Ciprofolxacin, 82804-260 — Ciprofloxacin Hydrochloride, 82868-070 — Ciprofloxacin Hydrochloride, 82868-102 — ciprofloxacin, 83008-078 — Ciprofolxacin, 83939-0002 — Ciprofloxacin Hydrochloride, 85293-003 — ciprofloxacin, 85293-004 — ciprofloxacin, 85534-0047 — Ciprofloxacin Hydrochloride, 85534-0069 — Ciprofloxacin Hydrochloride, 85534-0075 — Ciprofloxacin, 85534-0081 — Ciprofloxacin Hydrochloride, 85766-023 — Ciprofloxacin, 85766-099 — Ciprofolxacin, 85766-100 — Ciprofolxacin, 85766-245 — Ciprofloxacin and Dexamethasone, +195 more

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