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Ciprofloxacin

NDC 0143-9929 · Hikma Pharmaceuticals USA Inc.

Generic nameCiprofloxacin
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)CIPROFLOXACIN HYDROCHLORIDE
Strength750 mg/1
Pharmacologic classCytochrome P450 1A2 Inhibitors [MoA], Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]
Marketing categoryANDA

Packages

0143-9929-01 — 100 TABLET, FILM COATED in 1 BOTTLE (0143-9929-01)

0143-9929-50 — 50 TABLET, FILM COATED in 1 BOTTLE (0143-9929-50)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0143-9927 — Ciprofloxacin, 0143-9928 — Ciprofloxacin, 0615-8630 — Ciprofloxacin Hydrochloride, 0713-0851 — ciprofloxacin hydrochloride and hydrocortisone, 0781-6186 — ciprofloxacin and dexamethasone, 0781-6218 — ciprofloxacin hydrochloride and hydrocortisone, 0832-1430 — Ciprofloxacin Hydrochloride and Dexamethasone, 0904-7243 — ciprofloxacin, 16252-515 — Ciprofloxacin, 16571-411 — ciprofloxacin, 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, +195 more

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