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Ciprofloxacin

NDC 51407-165 · Golden State Medical Supply, Inc.

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

51407-165-01 — 100 TABLET, FILM COATED in 1 BOTTLE (51407-165-01)

51407-165-20 — 20 TABLET, FILM COATED in 1 BOTTLE (51407-165-20)

51407-165-28 — 28 TABLET, FILM COATED in 1 BOTTLE (51407-165-28)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50090-4600 — Ciprofloxacin Hydrochloride, 50090-5373 — Ciprofloxacin Hydrochloride, 50090-6043 — ciprofloxacin hydrochloride and hydrocortisone, 50090-7297 — Ciprofolxacin, 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, 51407-775 — 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, 58657-675 — Ciprofloxacin, +195 more

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