NDC 71335-1656 – Allopurinol

Allopurinol 100 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-1656

Product details

Brand name
Allopurinol
Generic name
Allopurinol
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA071586
Marketed since
October 1, 2009
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
71335-1656-1100 TABLET in 1 BOTTLE (71335-1656-1)Jan 30, 2025
71335-1656-230 TABLET in 1 BOTTLE (71335-1656-2)Sep 21, 2020
71335-1656-360 TABLET in 1 BOTTLE (71335-1656-3)Nov 11, 2020
71335-1656-4120 TABLET in 1 BOTTLE (71335-1656-4)Jan 30, 2025
71335-1656-520 TABLET in 1 BOTTLE (71335-1656-5)Jan 30, 2025
71335-1656-690 TABLET in 1 BOTTLE (71335-1656-6)Jun 29, 2020

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