PlainRecalls
FDA Drug Low Class III Terminated

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: 59011-256-30.

Reported: April 13, 2016 Initiated: March 31, 2016 #D-0810-2016

Product Description

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: 59011-256-30.

Reason for Recall

Failed Dissolution Specifications

Details

Recalling Firm
Purdue Pharma L.P.
Units Affected
2172 Cartons
Distribution
U.S. Including: FL, LA, MI, MS, NC, NJ, OH and SC.
Location
Stamford, CT

Frequently Asked Questions

What product was recalled?
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: 59011-256-30.. Recalled by Purdue Pharma L.P.. Units affected: 2172 Cartons.
Why was this product recalled?
Failed Dissolution Specifications
Which agency issued this recall?
This recall was issued by the FDA Drug on April 13, 2016. Severity: Low. Recall number: D-0810-2016.