Xanax (Alprazolam) USP recall: Labeling Error
Xanax (Alprazolam) USP, CIV, 0.5 mg tablets , 10 x 10 blister cards per carton, Rx Only, Manufactured by Sandoz Inc., Princeton, NJ 08805, NDC…
Why was Xanax (Alprazolam) USP recalled?
Labeling: Missing Label-Primary packaging label (i.e. blister card) is blank and contains no product information (e.g. product name, strength, lot number, expiry).
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 #: 0111512; Exp. 08/17
- Product
- Xanax (Alprazolam) USP, CIV, 0.5 mg tablets , 10 x 10 blister cards per carton, Rx Only, Manufactured by Sandoz Inc., Princeton, NJ 08805, NDC…
- Recalling firm
- Mckesson Packaging Services
- Quantity
- 3,492 unit cartons of 10 x 10 blister cards
- Distribution
- CO, IL, LA, OH
- Recall date
- October 5, 2016
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)