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Ciprofloxacin

NDC 76420-214 · Asclemed USA, Inc.

Generic nameCiprofloxacin
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)CIPROFLOXACIN HYDROCHLORIDE
Strength250 mg/1
Pharmacologic classQuinolone Antimicrobial [EPC], Quinolones [CS]
Marketing categoryANDA

Packages

76420-214-06 — 6 TABLET, FILM COATED in 1 BOTTLE (76420-214-06)

76420-214-10 — 10 TABLET, FILM COATED in 1 BOTTLE (76420-214-10)

76420-214-14 — 14 TABLET, FILM COATED in 1 BOTTLE (76420-214-14)

76420-214-20 — 20 TABLET, FILM COATED in 1 BOTTLE (76420-214-20)

76420-214-30 — 30 TABLET, FILM COATED in 1 BOTTLE (76420-214-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72789-124 — Ciprofloxacin, 72789-125 — Ciprofloxacin, 72789-193 — Ciprofloxacin, 72789-330 — Ciprofloxacin Hydrochloride, 72789-511 — Ciprofloxacin Hydrochloride, 72789-519 — Ciprofolxacin, 72789-520 — Ciprofloxacin Hydrochloride, 72789-577 — Ciprofloxacin Hydrochloride, 72888-102 — CIPROFLOXACIN HYDROCHLORIDE, 76420-045 — Ciprofloxacin Hydrochloride, 76420-273 — ciprofloxacin hydrochloride and hydrocortisone, 76420-588 — Ciprofloxacin, 76420-928 — Ciprofolxacin, 76420-929 — Ciprofolxacin, 76420-942 — Ciprofloxacin Hydrochloride, 80425-0192 — Ciprofloxacin HCL, 80425-0492 — Ciprofolxacin, 80425-0493 — Ciprofloxacin Hydrochloride, 80425-0499 — Ciprofloxacin, 82804-130 — Ciprofolxacin, +195 more

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