NDC 71335-3154 – Allopurinol

Allopurinol 300 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-3154

Product details

Brand name
Allopurinol
Generic name
Allopurinol
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA204467
Marketed since
October 31, 2023
Listing expires
December 31, 2027
Pharmacologic class
Xanthine Oxidase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Allopurinol →

Package NDC codes (5)

Package NDCDescriptionSince
71335-3154-130 TABLET in 1 BOTTLE (71335-3154-1)Jul 13, 2026
71335-3154-260 TABLET in 1 BOTTLE (71335-3154-2)Jul 13, 2026
71335-3154-3100 TABLET in 1 BOTTLE (71335-3154-3)Jul 13, 2026
71335-3154-490 TABLET in 1 BOTTLE (71335-3154-4)Jul 13, 2026
71335-3154-520 TABLET in 1 BOTTLE (71335-3154-5)Jul 13, 2026

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