NDC 68788-4027 – Allopurinol

Allopurinol 100 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68788-4027

Product details

Brand name
Allopurinol
Generic name
Allopurinol
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA217748
Marketed since
September 22, 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
68788-4027-1100 TABLET in 1 BOTTLE (68788-4027-1)Sep 22, 2025
68788-4027-330 TABLET in 1 BOTTLE (68788-4027-3)Sep 22, 2025
68788-4027-660 TABLET in 1 BOTTLE (68788-4027-6)Sep 22, 2025
68788-4027-990 TABLET in 1 BOTTLE (68788-4027-9)Sep 22, 2025

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