Ciprofloxacin

NDC 83008-078 · Quality Care Products, LLC

FDA lists marketing as ended on 2026-08-31.

Generic nameCiprofolxacin

Dosage formTABLET

RouteORAL

Active ingredient(s)CIPROFLOXACIN HYDROCHLORIDE

Strength500 mg/1

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

Marketing categoryANDA

Packages

83008-078-20 — 20 TABLET in 1 BOTTLE (83008-078-20)

FDA lists these products with the same active ingredient.

76420-942 — Ciprofloxacin Hydrochloride, 80425-0192 — Ciprofloxacin HCL, 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, 83939-0002 — Ciprofloxacin Hydrochloride, 85293-002 — ciprofloxacin, 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, +195 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.