Skip to main content

Ciprofloxacin

NDC 68788-8136 · Preferred Pharmaceuticals Inc.

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

Packages

68788-8136-0 — 6 TABLET, FILM COATED in 1 BOTTLE (68788-8136-0)

68788-8136-1 — 14 TABLET, FILM COATED in 1 BOTTLE (68788-8136-1)

68788-8136-2 — 20 TABLET, FILM COATED in 1 BOTTLE (68788-8136-2)

68788-8136-3 — 30 TABLET, FILM COATED in 1 BOTTLE (68788-8136-3)

68788-8136-8 — 10 TABLET, FILM COATED in 1 BOTTLE (68788-8136-8)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68071-3901 — Ciprofolxacin, 68071-3977 — Ciprofloxacin and dexamethasone, 68071-4122 — ciprofloxacin, 68071-4139 — Ciprofloxacin Hydrochloride, 68071-4235 — Ciprofloxacin Hydrochloride, 68071-4260 — ciprofloxacin, 68071-4672 — Ciprofloxacin, 68071-4679 — Ciprofloxacin, 68788-4177 — Ciprofloxacin Hydrochloride, 68788-7500 — Ciprofloxacin, 68788-8198 — Ciprofloxacin Hydrochloride, 68788-8200 — Ciprofloxacin, 68788-8692 — Ciprofolxacin, 68788-8875 — Ciprofolxacin, 69117-0008 — Ciprofloxacin Tablets, 69117-0009 — Ciprofloxacin Tablets, 69238-2432 — Ciprofloxacin, 69238-2433 — Ciprofloxacin, 69238-2434 — Ciprofloxacin, 69315-308 — 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.