Amlodipine Besylate Tablets
Subpotent Drug: Out-of-Specification test results observed in assay test at 21-month long term stability study.
18,003 recalls, newest first
Subpotent Drug: Out-of-Specification test results observed in assay test at 21-month long term stability study.
Presence of Foreign Substance: Presence of a small piece of blue plastic embedded in the tablet.
Failed Stability Specifications
Failed Stability Specification and Failed Impurities/Degradation Specifications: out of specification for inactive content ascorbic acid and MTHFRC-7impurity test
CGMP Deviations: use of non-food grade lubricant in mixing vessel.
CGMP Deviations: use of non-food grade lubricant in mixing vessel.
Failed Stability Specifications
Failed Dissolution Specifications: this repackaged product was recalled by the manufacturer, Dr. Reddy's Laboratories, Inc., due to out of specification results for dissolution.
Defective Delivery System
Failed dissolution specification: Out of specification results observed in 24-month long term stability testing.
Packaging defect: blister packaging inadequately sealed.
CGMP Deviations: good manufacturing deficiencies related to a lack of documentation of the fill line.
CGMP Deviations: good manufacturing deficiencies related to a lack of documentation of the fill line.
Failed Impurities/Degradation Specifications: Out of specification results obtained for conductivity.
cGMP deviations: potential for Microbial Contamination of Non-Sterile Products
Failed Impurities/Degradation Specifications: Out of specification results obtained for conductivity.
Labeling: Label Mix-up
cGMP deviations
cGMP deviations
cGMP deviations
cGMP deviations
cGMP deviations
cGMP deviations
cGMP deviations
cGMP deviations