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Ciprofloxacin Hydrochloride

NDC 68788-4177 · 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

68788-4177-0 — 6 TABLET, FILM COATED in 1 BOTTLE (68788-4177-0)

68788-4177-1 — 14 TABLET, FILM COATED in 1 BOTTLE (68788-4177-1)

68788-4177-2 — 20 TABLET, FILM COATED in 1 BOTTLE (68788-4177-2)

68788-4177-3 — 30 TABLET, FILM COATED in 1 BOTTLE (68788-4177-3)

68788-4177-8 — 10 TABLET, FILM COATED in 1 BOTTLE (68788-4177-8)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68071-3737 — Ciprofolxacin, 68071-3804 — Ciprofloxacin and Dexamethasone, 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, 68788-7500 — Ciprofloxacin, 68788-8136 — Ciprofloxacin Hydrochloride, 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, +195 more

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

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels