NDC 71335-2347 – Allopurinol

Allopurinol 100 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2347

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 (6)

Package NDCDescriptionSince
71335-2347-1100 TABLET in 1 BOTTLE (71335-2347-1)May 22, 2024
71335-2347-230 TABLET in 1 BOTTLE (71335-2347-2)Mar 14, 2024
71335-2347-360 TABLET in 1 BOTTLE (71335-2347-3)May 22, 2024
71335-2347-4120 TABLET in 1 BOTTLE (71335-2347-4)May 22, 2024
71335-2347-520 TABLET in 1 BOTTLE (71335-2347-5)May 22, 2024
71335-2347-690 TABLET in 1 BOTTLE (71335-2347-6)Mar 7, 2024

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