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Ciprofloxacin

NDC 71335-2450 · Bryant Ranch Prepack

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

71335-2450-0 7 TABLET in 1 BOTTLE (71335-2450-0)

71335-2450-1 14 TABLET in 1 BOTTLE (71335-2450-1)

71335-2450-2 30 TABLET in 1 BOTTLE (71335-2450-2)

71335-2450-3 20 TABLET in 1 BOTTLE (71335-2450-3)

71335-2450-4 60 TABLET in 1 BOTTLE (71335-2450-4)

71335-2450-5 6 TABLET in 1 BOTTLE (71335-2450-5)

71335-2450-6 10 TABLET in 1 BOTTLE (71335-2450-6)

71335-2450-7 28 TABLET in 1 BOTTLE (71335-2450-7)

71335-2450-8 100 TABLET in 1 BOTTLE (71335-2450-8)

71335-2450-9 40 TABLET in 1 BOTTLE (71335-2450-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71335-0070 — ciprofloxacin, 71335-0408 — ciprofloxacin, 71335-1024 — Ciprofloxacin Hydrochloride, 71335-1152 — Ciprofloxacin Tablets, 71335-1229 — Ciprofloxacin Tablets, 71335-1347 — Ciprofloxacin Hydrochloride, 71335-1867 — Ciprofloxacin, 71335-2046 — Ciprofloxacin Hydrochloride, 71335-2054 — Ciprofloxacin, 71335-2097 — Ciprofloxacin, 71335-2502 — Ciprofolxacin, 71610-081 — Ciprofloxacin, 71610-109 — Ciprofloxacin Hydrochloride, 71610-159 — Ciprofloxacin Hydrochloride, 72162-1740 — Ciprofloxacin Hydrochloride, 72162-1741 — Ciprofloxacin Hydrochloride, 72162-2425 — Ciprofolxacin, 72189-111 — ciprofloxacin hydrochloride, 72189-300 — CIPROFLOXACIN, 72189-304 — 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.