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Teva Issues Voluntary Nationwide Recall of One Lot of Anagrelide Capsules, USP 0.5 mg Due to Dissolution Test Failure | FDA
Teva Recalls One Lot of Anagrelide Capsules, USP 0.5 mg Due to Dissolution Test Failure | American Pharmaceutical Review - The Review of American Pharmaceutical Business & Technology
Teva Pharma Recalls One Lot Of Anagrelide Capsules
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FDA announces recall of platelet-reducing medication due to risk of clotting or other adverse cardiovascular outcomes
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FDA announces recall of platelet-reducing medication due to risk of clotting or other adverse cardiovascular outcomes
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These highlights do not include all the information needed to use ANAGRELIDE CAPSULES safely and effectively. See full prescribing information for ANAGRELIDE CAPSULES. ANAGRELIDE capsules, for oral useInitial U.S. Approval: 1997
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Torrent Pharmaceuticals Recall Anagrelide Capsules over drug's Dissolution test Failure • Drugwatcher.org
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Dissolution Test Failure Prompts Recall of Anagrelide Capsules - MPR
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