NDC 71335-2744 – Allopurinol

Allopurinol 100 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2744

Product details

Brand name
Allopurinol
Generic name
Allopurinol
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA217748
Marketed since
August 3, 2023
Listing expires
December 31, 2026
Pharmacologic class
Xanthine Oxidase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Allopurinol →

Package NDC codes (6)

Package NDCDescriptionSince
71335-2744-1100 TABLET in 1 BOTTLE (71335-2744-1)Oct 2, 2025
71335-2744-230 TABLET in 1 BOTTLE (71335-2744-2)Oct 2, 2025
71335-2744-360 TABLET in 1 BOTTLE (71335-2744-3)Oct 2, 2025
71335-2744-4120 TABLET in 1 BOTTLE (71335-2744-4)Oct 2, 2025
71335-2744-520 TABLET in 1 BOTTLE (71335-2744-5)Oct 2, 2025
71335-2744-690 TABLET in 1 BOTTLE (71335-2744-6)Oct 2, 2025

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