NDC 16729-134 – Allopurinol

Allopurinol 100 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC16729-134

Product details

Brand name
Allopurinol
Generic name
allopurinol
Labeler
Accord Healthcare 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 (2)

Package NDCDescriptionSince
16729-134-01100 TABLET in 1 BOTTLE (16729-134-01)Apr 29, 2015
16729-134-16500 TABLET in 1 BOTTLE (16729-134-16)Jun 14, 2016

Recalls mentioning this NDC

Other Allopurinol products