NDC 68788-8364 – Allopurinol

Allopurinol 300 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68788-8364

Product details

Brand name
Allopurinol
Generic name
Allopurinol
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA204467
Marketed since
February 1, 2023
Listing expires
December 31, 2026
Pharmacologic class
Xanthine Oxidase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Allopurinol →

Package NDC codes (3)

Package NDCDescriptionSince
68788-8364-1100 TABLET in 1 BOTTLE (68788-8364-1)Feb 1, 2023
68788-8364-330 TABLET in 1 BOTTLE (68788-8364-3)Feb 1, 2023
68788-8364-990 TABLET in 1 BOTTLE (68788-8364-9)Feb 1, 2023

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