NDC 42708-192 – Ciprofloxacin

Ciprofloxacin Hydrochloride 500 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC42708-192

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin
Labeler
QPharma, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076639
Marketed since
September 10, 2004
Listing expires
December 31, 2026
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Ciprofloxacin →

Package NDC codes (1)

Package NDCDescriptionSince
42708-192-14 sample14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42708-192-14)Oct 17, 2025

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