NDC 71335-9634 – Allopurinol

Allopurinol 300 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-9634

Product details

Brand name
Allopurinol
Generic name
Allopurinol
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA204467
Marketed since
September 22, 2020
Marketing end
October 31, 2029
Pharmacologic class
Xanthine Oxidase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Allopurinol →

Package NDC codes (5)

Package NDCDescriptionSince
71335-9634-130 TABLET in 1 BOTTLE (71335-9634-1)Mar 13, 2023
71335-9634-260 TABLET in 1 BOTTLE (71335-9634-2)Apr 15, 2026
71335-9634-3100 TABLET in 1 BOTTLE (71335-9634-3)Jan 4, 2024
71335-9634-490 TABLET in 1 BOTTLE (71335-9634-4)Apr 16, 2024
71335-9634-520 TABLET in 1 BOTTLE (71335-9634-5)Apr 15, 2026

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