NDC 51655-968 – Allopurinol

Allopurinol 300 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC51655-968

Product details

Brand name
Allopurinol
Generic name
Allopurinol
Labeler
Northwind Health Company, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA071450
Marketed since
April 8, 2022
Listing expires
December 31, 2027
Pharmacologic class
Xanthine Oxidase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Allopurinol →

Package NDC codes (2)

Package NDCDescriptionSince
51655-968-2690 TABLET in 1 BOTTLE, PLASTIC (51655-968-26)Jun 2, 2022
51655-968-5230 TABLET in 1 BOTTLE, PLASTIC (51655-968-52)Apr 8, 2022

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