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Ciprofloxacin

NDC 60760-676 · St. Mary's Medical Park Pharmacy

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

Packages

60760-676-10 — 10 TABLET, COATED in 1 BOTTLE, PLASTIC (60760-676-10)

60760-676-20 — 20 TABLET, COATED in 1 BOTTLE, PLASTIC (60760-676-20)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

59390-217 — Ciprofloxacin Hydrochloride, 59651-866 — Ciprofloxacin Hydrochloride, 59651-867 — Ciprofloxacin Hydrochloride, 59651-873 — Ciprofloxacin Hydrochloride, 59651-976 — Ciprofloxacin Hydrochloride, 59651-977 — Ciprofloxacin Hydrochloride, 59651-978 — Ciprofloxacin Hydrochloride, 60429-042 — Ciprofloxacin, 60687-860 — Ciprofloxacin Hydrochloride, 60687-947 — Ciprofloxacin Hydrochloride, 60760-689 — Ciprofolxacin, 60760-690 — Ciprofloxacin, 61314-656 — Ciprofloxacin Hydrochloride, 61442-222 — Ciprofloxacin Hydrochloride, 61442-223 — Ciprofloxacin Hydrochloride, 61442-224 — Ciprofloxacin Hydrochloride, 62135-308 — Ciprofloxacin hydrochloride, 62135-309 — Ciprofloxacin hydrochloride, 62135-310 — Ciprofloxacin hydrochloride, 62756-427 — Ciprofloxacin and dexamethasone, +195 more

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