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Ciprofloxacin HCL

NDC 80425-0192 · Advanced Rx Pharmacy of Tennessee, LLC

Generic nameCiprofloxacin HCL
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

80425-0192-1 — 20 TABLET, FILM COATED in 1 BOTTLE (80425-0192-1)

80425-0192-2 — 30 TABLET, FILM COATED in 1 BOTTLE (80425-0192-2)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72789-520 — Ciprofloxacin Hydrochloride, 72789-577 — Ciprofloxacin Hydrochloride, 72888-102 — CIPROFLOXACIN HYDROCHLORIDE, 76420-045 — Ciprofloxacin Hydrochloride, 76420-214 — Ciprofloxacin, 76420-273 — ciprofloxacin hydrochloride and hydrocortisone, 76420-588 — Ciprofloxacin, 76420-928 — Ciprofolxacin, 76420-929 — Ciprofolxacin, 76420-942 — Ciprofloxacin Hydrochloride, 80425-0492 — Ciprofolxacin, 80425-0493 — Ciprofloxacin Hydrochloride, 80425-0499 — Ciprofloxacin, 82804-130 — Ciprofolxacin, 82804-256 — Ciprofolxacin, 82804-260 — Ciprofloxacin Hydrochloride, 82868-070 — Ciprofloxacin Hydrochloride, 82868-102 — ciprofloxacin, 83008-078 — Ciprofolxacin, 83939-0002 — 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.