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Ciprofloxacin

NDC 85534-0069 · HAWAII REPACK, INC.

Generic nameCiprofloxacin Hydrochloride
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)CIPROFLOXACIN HYDROCHLORIDE
Strength250 mg/1
Pharmacologic classCytochrome P450 1A2 Inhibitors [MoA], Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]
Marketing categoryANDA

Packages

85534-0069-0 6 TABLET, FILM COATED in 1 BOTTLE (85534-0069-0)

85534-0069-1 10 TABLET, FILM COATED in 1 BOTTLE (85534-0069-1)

85534-0069-2 14 TABLET, FILM COATED in 1 BOTTLE (85534-0069-2)

85534-0069-3 20 TABLET, FILM COATED in 1 BOTTLE (85534-0069-3)

85534-0069-4 21 TABLET, FILM COATED in 1 BOTTLE (85534-0069-4)

85534-0069-5 28 TABLET, FILM COATED in 1 BOTTLE (85534-0069-5)

85534-0069-6 30 TABLET, FILM COATED in 1 BOTTLE (85534-0069-6)

Related Codes

Same active ingredient

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, 85293-002 — ciprofloxacin, 85293-003 — ciprofloxacin, 85293-004 — ciprofloxacin, 85534-0047 — 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.