Allopurinol Tablets recall
ALLOPURINOL TABLETS, USP, 300 mg, 500 count bottle, Rx only, Manufactured for: QUALITEST PHARMACEUTICALS, HUNTSVILLE, AL 35811 --- NDC 0603-2116-28
Why was Allopurinol Tablets recalled?
Failed Tablet/Capsule Specifications; report of oversized and discolored tablets
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
CP0761501, Exp. 12/16
- Product
- ALLOPURINOL TABLETS, USP, 300 mg, 500 count bottle, Rx only, Manufactured for: QUALITEST PHARMACEUTICALS, HUNTSVILLE, AL 35811 --- NDC 0603-2116-28
- Recalling firm
- Qualitest Pharmaceuticals
- Quantity
- 21552 units
- Distribution
- Nationwide and PR
- Recall date
- September 9, 2015
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)