1)
Citalopram Hydrobromide Tablets, 10 mg, NDC # 57664-507-13,
Lot #: 82577A - This lot is being recalled because some of the
tablets are oversized or undersized, which will result in
patients not receiving the expected dose.
2) Citalopram Hydrobromide Tablets, 40 mg, NDC # 57664-509-88,
Lot # 81940A - This lot is being recalled because it does not
meet manufacturing standards.
For more information, please visit:
http://www.fda.gov/Safety/Recalls/EnforcementReports/ucm170893.