Niacin Extended Release Tablets recall
Niacin Extended Release Tablets, USP, 500 mg, 90 count bottle, Rx Only, Teva Pharmaceuticals USA, Inc., Sellersville, PA, 18960, NDC 0093-7392-98
Why was Niacin Extended Release Tablets recalled?
Failed Tablet/Capsule Specifications: There is a potential for broken 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?
Lot#: 32900349B, Exp: 12/2014
- Product
- Niacin Extended Release Tablets, USP, 500 mg, 90 count bottle, Rx Only, Teva Pharmaceuticals USA, Inc., Sellersville, PA, 18960, NDC 0093-7392-98
- Recalling firm
- Teva Pharmaceuticals USA
- Quantity
- 10,512 bottles
- Distribution
- Nationwide and Puerto Rico, American Samoa, Virgin Islands, and Canal Zone
- Recall date
- January 8, 2014
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)