NDC 71335-0434 – Levofloxacin

Levofloxacin 500 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-0434

Product details

Brand name
Levofloxacin
Generic name
Levofloxacin
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA202801
Marketed since
January 9, 2015
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Levofloxacin →

Package NDC codes (10)

Package NDCDescriptionSince
71335-0434-090 TABLET, FILM COATED in 1 BOTTLE (71335-0434-0)Apr 3, 2024
71335-0434-130 TABLET, FILM COATED in 1 BOTTLE (71335-0434-1)May 7, 2018
71335-0434-210 TABLET, FILM COATED in 1 BOTTLE (71335-0434-2)Apr 19, 2018
71335-0434-37 TABLET, FILM COATED in 1 BOTTLE (71335-0434-3)Sep 5, 2018
71335-0434-414 TABLET, FILM COATED in 1 BOTTLE (71335-0434-4)Mar 5, 2018
71335-0434-55 TABLET, FILM COATED in 1 BOTTLE (71335-0434-5)Mar 30, 2018
71335-0434-620 TABLET, FILM COATED in 1 BOTTLE (71335-0434-6)Feb 13, 2018
71335-0434-760 TABLET, FILM COATED in 1 BOTTLE (71335-0434-7)Feb 14, 2018
71335-0434-83 TABLET, FILM COATED in 1 BOTTLE (71335-0434-8)Mar 10, 2022
71335-0434-950 TABLET, FILM COATED in 1 BOTTLE (71335-0434-9)Apr 21, 2021

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