NDC 80425-0492 – Ciprofloxacin

Ciprofloxacin Hydrochloride 500 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC80425-0492

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofolxacin
Labeler
Advanced Rx of Tennessee, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA208921
Marketed since
February 2, 2025
Listing expires
December 31, 2026
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for ciprofloxacin →

Package NDC codes (2)

Package NDCDescriptionSince
80425-0492-120 TABLET in 1 BOTTLE (80425-0492-1)Feb 2, 2025
80425-0492-230 TABLET in 1 BOTTLE (80425-0492-2)Feb 2, 2025

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