Intermezzo recall: Failed Dissolution
Intermezzo (zolpidem tartrate) sublingual tablet 1.75 mg, CIV, 30 Ct Cartons, Rx Only. Dist by Purdue Pharma L.P., Stamford, CT 06901-3431. NDC…
Why was Intermezzo recalled?
Failed Dissolution Specifications
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 #: 3126431B, Expiry: 09/30/17
- Product
- Intermezzo (zolpidem tartrate) sublingual tablet 1.75 mg, CIV, 30 Ct Cartons, Rx Only. Dist by Purdue Pharma L.P., Stamford, CT 06901-3431. NDC…
- Recalling firm
- Purdue Pharma L.P.
- Quantity
- 2172 Cartons
- Distribution
- U.S. Including: FL, LA, MI, MS, NC, NJ, OH and SC.
- Recall date
- April 13, 2016
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)