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Ciprofloxacin

NDC 51655-216 · Northwind Health Company, LLC

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

51655-216-20 — 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-216-20)

51655-216-25 — 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-216-25)

51655-216-52 — 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-216-52)

51655-216-53 — 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-216-53)

51655-216-84 — 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-216-84)

51655-216-87 — 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-216-87)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50090-7581 — Ciprofloxacin Hydrochloride, 50090-7631 — ciprofloxacin hydrochloride and hydrocortisone, 50090-7843 — Ciprofloxacin Hydrochloride, 50090-7848 — Ciprofloxacin Hydrochloride, 50419-754 — ciprofloxacin hydrochloride, 50419-758 — ciprofloxacin hydrochloride, 51407-165 — Ciprofloxacin Hydrochloride, 51407-775 — Ciprofloxacin Hydrochloride, 51407-776 — Ciprofloxacin Hydrochloride, 51655-086 — Ciprofloxacin, 51655-490 — Ciprofloxacin, 53746-831 — Ciprofloxacin and Dexamethasone, 54348-662 — CIPROFLOXACIN, 54348-663 — CIPROFLOXACIN, 55154-0193 — ciprofloxacin, 58657-675 — Ciprofloxacin, 58657-676 — Ciprofloxacin, 59390-217 — Ciprofloxacin Hydrochloride, 59651-866 — Ciprofloxacin Hydrochloride, 59651-867 — 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.