Purdue Pharma L.P. recalls Intermezzo (zolpidem tartrate), sublingual tablet 3.5 mg, 1 tablet per pouch, 30 pouches per carton, Rx only, Distribut…
- Recall date
- July 13, 2015
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-1278-2015
- FDA classification
- Class III
- Brand / firm
- Purdue Pharma L.P.
- Sold / distributed
- Nationwide and Puerto Rico
Why it was recalled
Failed dissolution specifications
Class III means the product violates regulations but is not likely to cause harm.
What was recalled
Intermezzo (zolpidem tartrate), sublingual tablet 3.5 mg, 1 tablet per pouch, 30 pouches per carton, Rx only, Distributed by Purdue Pharma L.P. Stamford, CT 06901-3431, NDC 59011-265-30
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