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ciprofloxacin

NDC 71335-0070 · Bryant Ranch Prepack

Generic nameciprofloxacin
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

71335-0070-0 7 TABLET in 1 BOTTLE (71335-0070-0)

71335-0070-1 14 TABLET in 1 BOTTLE (71335-0070-1)

71335-0070-2 30 TABLET in 1 BOTTLE (71335-0070-2)

71335-0070-3 20 TABLET in 1 BOTTLE (71335-0070-3)

71335-0070-4 60 TABLET in 1 BOTTLE (71335-0070-4)

71335-0070-5 6 TABLET in 1 BOTTLE (71335-0070-5)

71335-0070-6 10 TABLET in 1 BOTTLE (71335-0070-6)

71335-0070-7 28 TABLET in 1 BOTTLE (71335-0070-7)

71335-0070-8 100 TABLET in 1 BOTTLE (71335-0070-8)

71335-0070-9 40 TABLET in 1 BOTTLE (71335-0070-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70518-3063 — Ciprofloxacin, 70518-4133 — Ciprofolxacin, 70518-4214 — Ciprofloxacin Hydrochloride, 70518-4229 — Ciprofolxacin, 70934-965 — Ciprofloxacin Hydrochloride, 71205-300 — Ciprofloxacin, 71205-636 — Ciprofloxacin Hydrochloride, 71205-649 — Ciprofloxacin Hydrochloride, 71205-749 — Ciprofloxacin, 71205-997 — Ciprofloxacin Hydrochloride, 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, 71335-2450 — Ciprofolxacin, +195 more

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