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Ciprofloxacin

NDC 71205-649 · Proficient Rx LP

Generic nameCiprofloxacin Hydrochloride
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)CIPROFLOXACIN HYDROCHLORIDE
Strength500 mg/1
Pharmacologic classCytochrome P450 1A2 Inhibitors [MoA], Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]
Marketing categoryANDA

Packages

71205-649-06 6 TABLET, FILM COATED in 1 BOTTLE (71205-649-06)

71205-649-07 7 TABLET, FILM COATED in 1 BOTTLE (71205-649-07)

71205-649-10 10 TABLET, FILM COATED in 1 BOTTLE (71205-649-10)

71205-649-14 14 TABLET, FILM COATED in 1 BOTTLE (71205-649-14)

71205-649-20 20 TABLET, FILM COATED in 1 BOTTLE (71205-649-20)

71205-649-30 30 TABLET, FILM COATED in 1 BOTTLE (71205-649-30)

71205-649-60 60 TABLET, FILM COATED in 1 BOTTLE (71205-649-60)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70244-033 — Ciprofloxacin and dexamethasone, 70518-1170 — Ciprofloxacin Hydrochloride, 70518-2837 — Ciprofloxacin, 70518-3063 — Ciprofloxacin, 70518-4133 — Ciprofolxacin, 70518-4214 — Ciprofloxacin Hydrochloride, 70518-4229 — Ciprofolxacin, 70934-965 — Ciprofloxacin Hydrochloride, 71205-300 — Ciprofloxacin, 71205-636 — Ciprofloxacin Hydrochloride, 71205-749 — Ciprofloxacin, 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, +195 more

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