NDC 66267-665 – Allopurinol

Allopurinol 100 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC66267-665

Product details

Brand name
Allopurinol
Generic name
Allopurinol
Labeler
NuCare Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA203154
Marketed since
April 29, 2015
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
66267-665-3030 TABLET in 1 BOTTLE (66267-665-30)Dec 28, 2016
66267-665-6060 TABLET in 1 BOTTLE (66267-665-60)Dec 28, 2016
66267-665-9090 TABLET in 1 BOTTLE (66267-665-90)Dec 28, 2016

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