NDC 16729-135 – Allopurinol

Allopurinol 300 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC16729-135

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
16729-135-01100 TABLET in 1 BOTTLE (16729-135-01)Apr 29, 2015
16729-135-16500 TABLET in 1 BOTTLE (16729-135-16)Apr 29, 2015

Recalls mentioning this NDC

Other Allopurinol products