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Ciprofloxacin

NDC 70934-965 · Denton Pharma, Inc. DBA Northwind Pharmaceuticals

FDA lists marketing as ended on 2026-08-31.
Generic nameCiprofloxacin Hydrochloride
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)CIPROFLOXACIN HYDROCHLORIDE
Strength500 mg/1
Pharmacologic classQuinolone Antimicrobial [EPC], Quinolones [CS]
Marketing categoryANDA

Packages

70934-965-06 — 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-965-06)

70934-965-14 — 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-965-14)

70934-965-20 — 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-965-20)

70934-965-30 — 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-965-30)

70934-965-60 — 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-965-60)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

69367-385 — Ciprofloxacin Hydrochloride, 69367-386 — Ciprofloxacin Hydrochloride, 69367-387 — Ciprofloxacin Hydrochloride, 70244-033 — Ciprofloxacin and dexamethasone, 70518-1170 — Ciprofloxacin Hydrochloride, 70518-2837 — Ciprofloxacin, 70518-3063 — Ciprofloxacin, 70518-4133 — Ciprofolxacin, 70518-4214 — Ciprofloxacin Hydrochloride, 70518-4229 — Ciprofolxacin, 71205-300 — Ciprofloxacin, 71205-636 — Ciprofloxacin Hydrochloride, 71205-649 — Ciprofloxacin Hydrochloride, 71205-749 — Ciprofloxacin, 71205-997 — Ciprofloxacin Hydrochloride, 71335-0070 — ciprofloxacin, 71335-0408 — ciprofloxacin, 71335-1024 — Ciprofloxacin Hydrochloride, 71335-1152 — Ciprofloxacin Tablets, 71335-1229 — Ciprofloxacin Tablets, +195 more

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