Skip to main content

Ciprofloxacin

NDC 69117-0009 · Yiling Pharmaceutical, Inc.

Generic nameCiprofloxacin Tablets
Dosage formTABLET, COATED
RouteORAL
Active ingredient(s)CIPROFLOXACIN HYDROCHLORIDE
Strength500 mg/1
Pharmacologic classCytochrome P450 1A2 Inhibitors [MoA], Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]
Marketing categoryANDA

Packages

69117-0009-1 — 500 TABLET, COATED in 1 BOTTLE (69117-0009-1)

69117-0009-2 — 100 TABLET, COATED in 1 BOTTLE (69117-0009-2)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68071-4672 — Ciprofloxacin, 68071-4679 — Ciprofloxacin, 68788-4177 — Ciprofloxacin Hydrochloride, 68788-7500 — Ciprofloxacin, 68788-8136 — Ciprofloxacin Hydrochloride, 68788-8198 — Ciprofloxacin Hydrochloride, 68788-8200 — Ciprofloxacin, 68788-8692 — Ciprofolxacin, 68788-8875 — Ciprofolxacin, 69117-0008 — Ciprofloxacin Tablets, 69238-2432 — Ciprofloxacin, 69238-2433 — Ciprofloxacin, 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, +195 more

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