NDC 72162-1741 – Ciprofloxacin

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

Human Prescription Drug

Product NDC72162-1741

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076126
Marketed since
October 10, 2009
Listing expires
December 31, 2026
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for ciprofloxacin →

Package NDC codes (8)

Package NDCDescriptionSince
72162-1741-1100 TABLET, FILM COATED in 1 BOTTLE (72162-1741-1)Oct 4, 2024
72162-1741-214 TABLET, FILM COATED in 1 BOTTLE (72162-1741-2)Oct 4, 2024
72162-1741-330 TABLET, FILM COATED in 1 BOTTLE (72162-1741-3)Oct 4, 2024
72162-1741-420 TABLET, FILM COATED in 1 BOTTLE (72162-1741-4)Oct 4, 2024
72162-1741-5500 TABLET, FILM COATED in 1 BOTTLE (72162-1741-5)Oct 4, 2024
72162-1741-660 TABLET, FILM COATED in 1 BOTTLE (72162-1741-6)Oct 4, 2024
72162-1741-710 TABLET, FILM COATED in 1 BOTTLE (72162-1741-7)Oct 4, 2024
72162-1741-8120 TABLET, FILM COATED in 1 BOTTLE (72162-1741-8)Oct 4, 2024

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