NDC 71335-1681 – Metronidazole

Metronidazole 500 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-1681

Product details

Brand name
Metronidazole
Generic name
Metronidazole
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA079067
Marketed since
December 1, 2016
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
71335-1681-040 TABLET in 1 BOTTLE (71335-1681-0)Oct 31, 2024
71335-1681-120 TABLET in 1 BOTTLE (71335-1681-1)Aug 5, 2020
71335-1681-230 TABLET in 1 BOTTLE (71335-1681-2)Aug 4, 2020
71335-1681-314 TABLET in 1 BOTTLE (71335-1681-3)Aug 5, 2020
71335-1681-456 TABLET in 1 BOTTLE (71335-1681-4)Oct 31, 2024
71335-1681-521 TABLET in 1 BOTTLE (71335-1681-5)Aug 10, 2020
71335-1681-64 TABLET in 1 BOTTLE (71335-1681-6)Jul 12, 2021
71335-1681-728 TABLET in 1 BOTTLE (71335-1681-7)Aug 31, 2020
71335-1681-8100 TABLET in 1 BOTTLE (71335-1681-8)Oct 31, 2024
71335-1681-960 TABLET in 1 BOTTLE (71335-1681-9)Oct 31, 2024

Other Metronidazole products