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ciprofloxacin

NDC 54348-662 · PharmPak, Inc.

Generic nameCIPROFLOXACIN
Dosage formTABLET
RouteORAL
Active ingredient(s)CIPROFLOXACIN HYDROCHLORIDE
Strength250 mg/1
Pharmacologic classQuinolone Antimicrobial [EPC], Quinolones [CS]
Marketing categoryANDA

Packages

54348-662-06 — 1 BOTTLE in 1 BOX (54348-662-06) / 6 TABLET in 1 BOTTLE

54348-662-14 — 1 BOTTLE in 1 BOX (54348-662-14) / 14 TABLET in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50090-7848 — Ciprofloxacin Hydrochloride, 50419-754 — ciprofloxacin hydrochloride, 50419-758 — ciprofloxacin hydrochloride, 51407-165 — Ciprofloxacin Hydrochloride, 51407-775 — Ciprofloxacin Hydrochloride, 51407-776 — Ciprofloxacin Hydrochloride, 51655-086 — Ciprofloxacin, 51655-216 — Ciprofloxacin Hydrochloride, 51655-490 — Ciprofloxacin, 53746-831 — Ciprofloxacin and Dexamethasone, 54348-663 — CIPROFLOXACIN, 55154-0193 — ciprofloxacin, 58657-675 — Ciprofloxacin, 58657-676 — Ciprofloxacin, 59390-217 — Ciprofloxacin Hydrochloride, 59651-866 — Ciprofloxacin Hydrochloride, 59651-867 — Ciprofloxacin Hydrochloride, 59651-873 — Ciprofloxacin Hydrochloride, 59651-976 — Ciprofloxacin Hydrochloride, 59651-977 — 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.