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Ciprofloxacin Hydrochloride

NDC 69367-385 · Westminster Pharmaceuticals, LLC

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

69367-385-01 — 100 TABLET, FILM COATED in 1 BOTTLE (69367-385-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68788-8198 — Ciprofloxacin Hydrochloride, 68788-8200 — Ciprofloxacin, 68788-8692 — Ciprofolxacin, 68788-8875 — Ciprofolxacin, 69117-0008 — Ciprofloxacin Tablets, 69117-0009 — Ciprofloxacin Tablets, 69238-2432 — Ciprofloxacin, 69238-2433 — Ciprofloxacin, 69238-2434 — Ciprofloxacin, 69315-308 — Ciprofloxacin, 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, 70518-4214 — Ciprofloxacin Hydrochloride, 70518-4229 — Ciprofolxacin, 70934-965 — 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.