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Ciprofloxacin

NDC 70518-4214 · REMEDYREPACK 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

70518-4214-0 — 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4214-0)

70518-4214-1 — 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4214-1)

70518-4214-2 — 14 TABLET, FILM COATED in 1 BLISTER PACK (70518-4214-2)

70518-4214-3 — 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4214-3)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

69238-2434 — Ciprofloxacin, 69315-308 — Ciprofloxacin, 69367-385 — Ciprofloxacin Hydrochloride, 69367-386 — Ciprofloxacin Hydrochloride, 69367-387 — Ciprofloxacin Hydrochloride, 70244-033 — Ciprofloxacin and dexamethasone, 70518-1170 — Ciprofloxacin Hydrochloride, 70518-2837 — Ciprofloxacin, 70518-3063 — Ciprofloxacin, 70518-4133 — Ciprofolxacin, 70518-4229 — Ciprofolxacin, 70934-965 — Ciprofloxacin Hydrochloride, 71205-300 — Ciprofloxacin, 71205-636 — Ciprofloxacin Hydrochloride, 71205-649 — Ciprofloxacin Hydrochloride, 71205-749 — Ciprofloxacin, 71205-997 — Ciprofloxacin Hydrochloride, 71335-0070 — ciprofloxacin, 71335-0408 — ciprofloxacin, 71335-1024 — 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.