NDC 71335-0358 – Metronidazole

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

Human Prescription Drug

Product NDC71335-0358

Product details

Brand name
Metronidazole
Generic name
Metronidazole
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA203458
Marketed since
June 1, 2014
Listing expires
December 31, 2026
Pharmacologic class
Nitroimidazole Antimicrobial

Active ingredients

Uses, dosage, side effects and warnings for Metronidazole →

Package NDC codes (10)

Package NDCDescriptionSince
71335-0358-040 TABLET, FILM COATED in 1 BOTTLE (71335-0358-0)Nov 7, 2018
71335-0358-120 TABLET, FILM COATED in 1 BOTTLE (71335-0358-1)Feb 27, 2018
71335-0358-230 TABLET, FILM COATED in 1 BOTTLE (71335-0358-2)Feb 20, 2018
71335-0358-314 TABLET, FILM COATED in 1 BOTTLE (71335-0358-3)Mar 28, 2018
71335-0358-456 TABLET, FILM COATED in 1 BOTTLE (71335-0358-4)Apr 5, 2024
71335-0358-521 TABLET, FILM COATED in 1 BOTTLE (71335-0358-5)Aug 3, 2018
71335-0358-64 TABLET, FILM COATED in 1 BOTTLE (71335-0358-6)Oct 26, 2018
71335-0358-728 TABLET, FILM COATED in 1 BOTTLE (71335-0358-7)May 29, 2018
71335-0358-8100 TABLET, FILM COATED in 1 BOTTLE (71335-0358-8)Jun 12, 2018
71335-0358-942 TABLET, FILM COATED in 1 BOTTLE (71335-0358-9)Jul 29, 2019

Other Metronidazole products