NDC 71335-1922 – Metronidazole

Metronidazole 500 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-1922

Product details

Brand name
Metronidazole
Generic name
Metronidazole
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA203974
Marketed since
May 29, 2015
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
71335-1922-040 TABLET in 1 BOTTLE (71335-1922-0)Oct 31, 2024
71335-1922-120 TABLET in 1 BOTTLE (71335-1922-1)Aug 11, 2021
71335-1922-230 TABLET in 1 BOTTLE (71335-1922-2)Aug 26, 2021
71335-1922-314 TABLET in 1 BOTTLE (71335-1922-3)Oct 7, 2021
71335-1922-456 TABLET in 1 BOTTLE (71335-1922-4)Oct 31, 2024
71335-1922-521 TABLET in 1 BOTTLE (71335-1922-5)Dec 9, 2021
71335-1922-64 TABLET in 1 BOTTLE (71335-1922-6)Oct 4, 2021
71335-1922-728 TABLET in 1 BOTTLE (71335-1922-7)Aug 3, 2021
71335-1922-8100 TABLET in 1 BOTTLE (71335-1922-8)Oct 31, 2024
71335-1922-960 TABLET in 1 BOTTLE (71335-1922-9)Oct 31, 2024

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