NDC 68788-8865 – Allopurinol

Allopurinol 300 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68788-8865

Product details

Brand name
Allopurinol
Generic name
Allopurinol
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA217748
Marketed since
April 23, 2025
Listing expires
December 31, 2026
Pharmacologic class
Xanthine Oxidase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Allopurinol →

Package NDC codes (4)

Package NDCDescriptionSince
68788-8865-1100 TABLET in 1 BOTTLE (68788-8865-1)Apr 23, 2025
68788-8865-330 TABLET in 1 BOTTLE (68788-8865-3)Apr 23, 2025
68788-8865-660 TABLET in 1 BOTTLE (68788-8865-6)Apr 23, 2025
68788-8865-990 TABLET in 1 BOTTLE (68788-8865-9)Apr 23, 2025

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