NDC 71335-9676 – Allopurinol

Allopurinol 300 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-9676

Product details

Brand name
Allopurinol
Generic name
Allopurinol
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA018659
Marketed since
October 24, 1986
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
71335-9676-130 TABLET in 1 BOTTLE (71335-9676-1)Jul 8, 2024
71335-9676-260 TABLET in 1 BOTTLE (71335-9676-2)Apr 13, 2026
71335-9676-3100 TABLET in 1 BOTTLE (71335-9676-3)Mar 13, 2024
71335-9676-490 TABLET in 1 BOTTLE (71335-9676-4)Apr 19, 2023
71335-9676-520 TABLET in 1 BOTTLE (71335-9676-5)Apr 13, 2026

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