NDC 71335-0112 – Allopurinol

Allopurinol 300 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0112

Product details

Brand name
Allopurinol
Generic name
Allopurinol
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA203154
Marketed since
April 29, 2015
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
71335-0112-130 TABLET in 1 BOTTLE (71335-0112-1)Apr 13, 2018
71335-0112-260 TABLET in 1 BOTTLE (71335-0112-2)May 16, 2018
71335-0112-3100 TABLET in 1 BOTTLE (71335-0112-3)Sep 18, 2018
71335-0112-490 TABLET in 1 BOTTLE (71335-0112-4)Apr 18, 2018
71335-0112-520 TABLET in 1 BOTTLE (71335-0112-5)Dec 27, 2021

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