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Ciprofloxacin

NDC 85766-099 · Sportpharm LLC

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

Packages

85766-099-01 — 100 TABLET in 1 BOTTLE (85766-099-01)

85766-099-10 — 10 TABLET in 1 BOTTLE (85766-099-10)

85766-099-20 — 20 TABLET in 1 BOTTLE (85766-099-20)

85766-099-30 — 30 TABLET in 1 BOTTLE (85766-099-30)

85766-099-60 — 60 TABLET in 1 BOTTLE (85766-099-60)

85766-099-90 — 90 TABLET in 1 BOTTLE (85766-099-90)

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, 85534-0069 — Ciprofloxacin Hydrochloride, 85534-0075 — Ciprofloxacin, 85534-0081 — Ciprofloxacin Hydrochloride, 85766-023 — Ciprofloxacin, 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.