NDC 68788-8727 – Allopurinol

Allopurinol 100 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68788-8727

Product details

Brand name
Allopurinol
Generic name
Allopurinol
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA214443
Marketed since
August 16, 2024
Listing expires
December 31, 2027
Pharmacologic class
Xanthine Oxidase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Allopurinol →

Package NDC codes (4)

Package NDCDescriptionSince
68788-8727-1100 TABLET in 1 BOTTLE (68788-8727-1)Aug 16, 2024
68788-8727-330 TABLET in 1 BOTTLE (68788-8727-3)Aug 16, 2024
68788-8727-660 TABLET in 1 BOTTLE (68788-8727-6)Aug 16, 2024
68788-8727-990 TABLET in 1 BOTTLE (68788-8727-9)Aug 16, 2024

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