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Ciprofloxacin

NDC 58657-675 · Method Pharmaceuticals, LLC

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

58657-675-01 — 100 TABLET, COATED in 1 BOTTLE (58657-675-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

51407-165 — Ciprofloxacin Hydrochloride, 51407-775 — Ciprofloxacin Hydrochloride, 51407-776 — Ciprofloxacin Hydrochloride, 51655-086 — Ciprofloxacin, 51655-216 — Ciprofloxacin Hydrochloride, 51655-490 — Ciprofloxacin, 53746-831 — Ciprofloxacin and Dexamethasone, 54348-662 — CIPROFLOXACIN, 54348-663 — CIPROFLOXACIN, 55154-0193 — ciprofloxacin, 58657-676 — Ciprofloxacin, 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, +195 more

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