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Ciprofloxacin

NDC 67296-2135 · Redpharm Drug

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

67296-2135-1 — 14 TABLET in 1 BOTTLE (67296-2135-1)

67296-2135-2 — 10 TABLET in 1 BOTTLE (67296-2135-2)

67296-2135-3 — 20 TABLET in 1 BOTTLE (67296-2135-3)

67296-2135-6 — 6 TABLET in 1 BOTTLE (67296-2135-6)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

66758-071 — ciprofloxacin hydrochloride, 66758-087 — ciprofloxacin hydrochloride and hydrocortisone, 67046-1460 — Ciprofolxacin, 67046-1528 — ciprofloxacin, 67046-1537 — Ciprofolxacin, 67046-1692 — Ciprofloxacin Hydrochloride, 67296-0142 — Ciprofloxacin Hydrochloride, 67296-1703 — Ciprofloxacin, 67296-1848 — Ciprofloxacin, 67296-1943 — Ciprofloxacin and dexamethasone, 67296-2169 — Ciprofolxacin, 67296-2208 — Ciprofloxacin Hydrochloride, 67296-2257 — Ciprofloxacin and Dexamethasone, 67296-2291 — Ciprofloxacin Hydrochloride, 68071-2267 — Ciprofloxacin, 68071-2269 — Ciprofloxacin, 68071-2383 — Ciprofloxacin, 68071-2384 — Ciprofloxacin, 68071-2404 — Ciprofloxacin, 68071-3351 — 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.