NDC 71335-2416 – Allopurinol

Allopurinol 100 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2416

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 (6)

Package NDCDescriptionSince
71335-2416-1100 TABLET in 1 BOTTLE (71335-2416-1)Nov 12, 2024
71335-2416-230 TABLET in 1 BOTTLE (71335-2416-2)Nov 12, 2024
71335-2416-360 TABLET in 1 BOTTLE (71335-2416-3)Nov 12, 2024
71335-2416-4120 TABLET in 1 BOTTLE (71335-2416-4)Nov 12, 2024
71335-2416-520 TABLET in 1 BOTTLE (71335-2416-5)Nov 12, 2024
71335-2416-690 TABLET in 1 BOTTLE (71335-2416-6)Nov 12, 2024

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