ciprofloxacin

NDC 50090-1648 · A-S Medication Solutions

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

50090-1648-0 20 TABLET in 1 BOTTLE (50090-1648-0)

50090-1648-1 14 TABLET in 1 BOTTLE (50090-1648-1)

50090-1648-3 6 TABLET in 1 BOTTLE (50090-1648-3)

50090-1648-4 28 TABLET in 1 BOTTLE (50090-1648-4)

50090-1648-5 10 TABLET in 1 BOTTLE (50090-1648-5)

50090-1648-7 30 TABLET in 1 BOTTLE (50090-1648-7)

50090-1648-8 1 TABLET in 1 BOTTLE (50090-1648-8)

FDA lists these products with the same active ingredient.

42708-192 — ciprofloxacin, 43063-410 — ciprofloxacin, 43063-547 — Ciprofloxacin, 43063-767 — ciprofloxacin, 43063-869 — ciprofloxacin, 43063-923 — Ciprofloxacin Hydrochloride, 43547-688 — Ciprofolxacin, 43547-689 — Ciprofolxacin, 43598-326 — Ciprofloxacin and Dexamethasone, 50090-0882 — Ciprofloxacin Hydrochloride, 50090-1649 — ciprofloxacin, 50090-1754 — Ciprofloxacin Hydrochloride, 50090-2146 — Ciprofloxacin Hydrochloride, 50090-3791 — Ciprofloxacin Hydrochloride, 50090-3852 — Ciprofloxacin Hydrochloride, 50090-4217 — Ciprofloxacin, 50090-4600 — Ciprofloxacin Hydrochloride, 50090-5373 — Ciprofloxacin Hydrochloride, 50090-6043 — ciprofloxacin hydrochloride and hydrocortisone, 50090-7297 — 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.