NDC 71335-1703 – Metronidazole

Metronidazole 500 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-1703

Product details

Brand name
Metronidazole
Generic name
Metronidazole
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA206560
Marketed since
February 23, 2019
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
71335-1703-040 TABLET in 1 BOTTLE (71335-1703-0)Nov 22, 2022
71335-1703-120 TABLET in 1 BOTTLE (71335-1703-1)Sep 23, 2020
71335-1703-230 TABLET in 1 BOTTLE (71335-1703-2)Oct 20, 2020
71335-1703-314 TABLET in 1 BOTTLE (71335-1703-3)Oct 5, 2020
71335-1703-456 TABLET in 1 BOTTLE (71335-1703-4)Aug 12, 2024
71335-1703-521 TABLET in 1 BOTTLE (71335-1703-5)Oct 16, 2020
71335-1703-64 TABLET in 1 BOTTLE (71335-1703-6)Nov 5, 2021
71335-1703-728 TABLET in 1 BOTTLE (71335-1703-7)Sep 24, 2020
71335-1703-8100 TABLET in 1 BOTTLE (71335-1703-8)Aug 12, 2024
71335-1703-960 TABLET in 1 BOTTLE (71335-1703-9)Apr 15, 2024

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