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Ciprofloxacin

NDC 71610-081 · Aphena Pharma Solutions - Tennessee, LLC

Generic nameCiprofloxacin
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)CIPROFLOXACIN HYDROCHLORIDE
Strength500 mg/1
Pharmacologic classQuinolone Antimicrobial [EPC], Quinolones [CS]
Marketing categoryANDA

Packages

71610-081-83 — 3600 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-081-83)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71335-1024 — Ciprofloxacin Hydrochloride, 71335-1152 — Ciprofloxacin Tablets, 71335-1229 — Ciprofloxacin Tablets, 71335-1347 — Ciprofloxacin Hydrochloride, 71335-1867 — Ciprofloxacin, 71335-2046 — Ciprofloxacin Hydrochloride, 71335-2054 — Ciprofloxacin, 71335-2097 — Ciprofloxacin, 71335-2450 — Ciprofolxacin, 71335-2502 — Ciprofolxacin, 71610-109 — Ciprofloxacin Hydrochloride, 71610-159 — Ciprofloxacin Hydrochloride, 72162-1740 — Ciprofloxacin Hydrochloride, 72162-1741 — Ciprofloxacin Hydrochloride, 72162-2425 — Ciprofolxacin, 72189-111 — ciprofloxacin hydrochloride, 72189-300 — CIPROFLOXACIN, 72189-304 — Ciprofloxacin, 72189-323 — CIPROFLOXACIN, 72189-616 — 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.