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ciprofloxacin

NDC 66267-716 · NuCare Pharmaceuticals, Inc.

Generic nameciprofloxacin
Dosage formTABLET
RouteORAL
Active ingredient(s)CIPROFLOXACIN HYDROCHLORIDE
Strength500 mg/1
Pharmacologic classCytochrome P450 1A2 Inhibitors [MoA], Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]
Marketing categoryANDA

Packages

66267-716-02 — 2 TABLET in 1 BOTTLE (66267-716-02)

66267-716-04 — 4 TABLET in 1 BOTTLE (66267-716-04)

66267-716-06 — 6 TABLET in 1 BOTTLE (66267-716-06)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

62756-427 — Ciprofloxacin and dexamethasone, 63187-017 — ciprofloxacin, 63187-142 — ciprofloxacin, 63187-985 — Ciprofloxacin Hydrochloride, 63187-990 — ciprofloxacin, 63629-1010 — Ciprofloxacin Hydrochloride, 63629-3868 — Ciprofloxacin, 65862-076 — Ciprofloxacin Hydrochloride, 65862-077 — Ciprofloxacin Hydrochloride, 65862-078 — Ciprofloxacin Hydrochloride, 66267-919 — ciprofloxacin, 66758-071 — ciprofloxacin hydrochloride, 66758-087 — ciprofloxacin hydrochloride and hydrocortisone, 67046-1460 — Ciprofolxacin, 67046-1528 — ciprofloxacin, 67046-1537 — Ciprofolxacin, 67046-1692 — Ciprofloxacin Hydrochloride, 67296-0142 — Ciprofloxacin Hydrochloride, 67296-1703 — Ciprofloxacin, 67296-1848 — 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.