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Ciprofloxacin

NDC 63629-3868 · Bryant Ranch Prepack

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

63629-3868-1 20 TABLET, FILM COATED in 1 BOTTLE (63629-3868-1)

63629-3868-2 28 TABLET, FILM COATED in 1 BOTTLE (63629-3868-2)

63629-3868-3 14 TABLET, FILM COATED in 1 BOTTLE (63629-3868-3)

63629-3868-4 30 TABLET, FILM COATED in 1 BOTTLE (63629-3868-4)

63629-3868-5 60 TABLET, FILM COATED in 1 BOTTLE (63629-3868-5)

63629-3868-6 10 TABLET, FILM COATED in 1 BOTTLE (63629-3868-6)

63629-3868-7 90 TABLET, FILM COATED in 1 BOTTLE (63629-3868-7)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

61442-224 — Ciprofloxacin Hydrochloride, 62135-308 — Ciprofloxacin hydrochloride, 62135-309 — Ciprofloxacin hydrochloride, 62135-310 — Ciprofloxacin hydrochloride, 62756-427 — Ciprofloxacin and dexamethasone, 63187-017 — ciprofloxacin, 63187-142 — ciprofloxacin, 63187-985 — Ciprofloxacin Hydrochloride, 63187-990 — ciprofloxacin, 63629-1010 — Ciprofloxacin Hydrochloride, 65862-076 — Ciprofloxacin Hydrochloride, 65862-077 — Ciprofloxacin Hydrochloride, 65862-078 — Ciprofloxacin Hydrochloride, 66267-716 — ciprofloxacin, 66267-919 — ciprofloxacin, 66758-071 — ciprofloxacin hydrochloride, 66758-087 — ciprofloxacin hydrochloride and hydrocortisone, 67046-1460 — Ciprofolxacin, 67046-1528 — ciprofloxacin, 67046-1537 — 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.