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Ciprofloxacin

NDC 71335-2097 · Bryant Ranch Prepack

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

Packages

71335-2097-0 7 TABLET, COATED in 1 BOTTLE (71335-2097-0)

71335-2097-1 20 TABLET, COATED in 1 BOTTLE (71335-2097-1)

71335-2097-2 10 TABLET, COATED in 1 BOTTLE (71335-2097-2)

71335-2097-3 14 TABLET, COATED in 1 BOTTLE (71335-2097-3)

71335-2097-4 6 TABLET, COATED in 1 BOTTLE (71335-2097-4)

71335-2097-5 30 TABLET, COATED in 1 BOTTLE (71335-2097-5)

71335-2097-6 60 TABLET, COATED in 1 BOTTLE (71335-2097-6)

71335-2097-7 12 TABLET, COATED in 1 BOTTLE (71335-2097-7)

71335-2097-8 40 TABLET, COATED in 1 BOTTLE (71335-2097-8)

71335-2097-9 90 TABLET, COATED in 1 BOTTLE (71335-2097-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71205-997 — Ciprofloxacin Hydrochloride, 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, 71335-2450 — Ciprofolxacin, 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, +195 more

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