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Ciprofloxacin

NDC 43547-688 · Solco Healthcare US, LLC

Generic nameCiprofolxacin
Dosage formTABLET
RouteORAL
Active ingredient(s)CIPROFLOXACIN HYDROCHLORIDE
Strength250 mg/1
Pharmacologic classCytochrome P450 1A2 Inhibitors [MoA], Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]
Marketing categoryANDA

Packages

43547-688-10 — 100 TABLET in 1 BOTTLE (43547-688-10)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

16571-412 — ciprofloxacin, 16571-413 — ciprofloxacin, 16714-628 — Ciprofloxacin and Dexamethasone, 42708-088 — Ciprofloxacin, 42708-192 — ciprofloxacin, 43063-410 — ciprofloxacin, 43063-547 — Ciprofloxacin, 43063-767 — ciprofloxacin, 43063-869 — ciprofloxacin, 43063-923 — Ciprofloxacin Hydrochloride, 43547-689 — Ciprofolxacin, 43598-326 — Ciprofloxacin and Dexamethasone, 50090-0882 — Ciprofloxacin Hydrochloride, 50090-1648 — ciprofloxacin, 50090-1649 — ciprofloxacin, 50090-1754 — Ciprofloxacin Hydrochloride, 50090-2146 — Ciprofloxacin Hydrochloride, 50090-3791 — Ciprofloxacin Hydrochloride, 50090-3852 — Ciprofloxacin Hydrochloride, 50090-4217 — 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.