NDC 71335-1347 – Ciprofloxacin

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

Human Prescription Drug

Product NDC71335-1347

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 (10)

Package NDCDescriptionSince
71335-1347-07 TABLET, FILM COATED in 1 BOTTLE (71335-1347-0)May 30, 2024
71335-1347-114 TABLET, FILM COATED in 1 BOTTLE (71335-1347-1)May 30, 2024
71335-1347-230 TABLET, FILM COATED in 1 BOTTLE (71335-1347-2)May 30, 2024
71335-1347-320 TABLET, FILM COATED in 1 BOTTLE (71335-1347-3)May 30, 2024
71335-1347-460 TABLET, FILM COATED in 1 BOTTLE (71335-1347-4)May 30, 2024
71335-1347-56 TABLET, FILM COATED in 1 BOTTLE (71335-1347-5)May 30, 2024
71335-1347-610 TABLET, FILM COATED in 1 BOTTLE (71335-1347-6)May 30, 2024
71335-1347-728 TABLET, FILM COATED in 1 BOTTLE (71335-1347-7)May 30, 2024
71335-1347-8100 TABLET, FILM COATED in 1 BOTTLE (71335-1347-8)May 30, 2024
71335-1347-940 TABLET, FILM COATED in 1 BOTTLE (71335-1347-9)May 30, 2024

Other ciprofloxacin products