NDC 71335-2332 – Allopurinol

Allopurinol 300 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2332

Product details

Brand name
Allopurinol
Generic name
Allopurinol
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA211820
Marketed since
March 12, 2019
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
71335-2332-130 TABLET in 1 BOTTLE, PLASTIC (71335-2332-1)Apr 3, 2024
71335-2332-260 TABLET in 1 BOTTLE, PLASTIC (71335-2332-2)Apr 3, 2024
71335-2332-3100 TABLET in 1 BOTTLE, PLASTIC (71335-2332-3)Mar 13, 2024
71335-2332-490 TABLET in 1 BOTTLE, PLASTIC (71335-2332-4)Apr 3, 2024
71335-2332-520 TABLET in 1 BOTTLE, PLASTIC (71335-2332-5)Apr 3, 2024

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