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Ciprofloxacin

NDC 65862-077 · Aurobindo Pharma Limited

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

65862-077-01 — 100 TABLET, FILM COATED in 1 BOTTLE (65862-077-01)

65862-077-05 — 500 TABLET, FILM COATED in 1 BOTTLE (65862-077-05)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

62135-309 — Ciprofloxacin hydrochloride, 62135-310 — Ciprofloxacin hydrochloride, 62756-427 — Ciprofloxacin and dexamethasone, 63187-017 — ciprofloxacin, 63187-142 — ciprofloxacin, 63187-985 — Ciprofloxacin Hydrochloride, 63187-990 — ciprofloxacin, 63629-1010 — Ciprofloxacin Hydrochloride, 63629-3868 — Ciprofloxacin, 65862-076 — Ciprofloxacin Hydrochloride, 65862-078 — Ciprofloxacin Hydrochloride, 66267-716 — ciprofloxacin, 66267-919 — ciprofloxacin, 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, +195 more

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