Class II
Drug Recall: Lithium Carbonate Extended-Release Tablets, USP, 300 mg, 100 Tablets per bottle, Rx only, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505. NDC: 0378-1300-01
CARDINAL HEALTHCARE · January 26, 2022
Reason for Recall
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Distribution
Nationwide USA
States Affected
NATIONWIDE
Quantity Affected
1 unit
Source: FDA (openFDA Drug Enforcement)
Recall number: D-0189-2024
Status: terminated
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.