Drug recall D-0429-2021
Product
Edarbi (azilsartan medoxomil) tablets 80 mg 30 Tablets Rx Only NDC 60631-080-30 Manufactured for: arbor Pharmaceuticals Atlanta, GA 30328
Reason for recall
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
Lots and codes
78902-1
Recall details
- Recalling firm
- Cardinal Health Inc., Dublin, OH
- Quantity
- 328 bottles
- Distribution
- FL, GA, SC
- Type
- Voluntary: Firm initiated
- Recall initiated
- March 15, 2021
- Terminated
- June 17, 2024
Related products
- Edarbi – drug information
- NDC 60631-080 Edarbi · Azilsartan Kamedoxomil 80 mg/1 · Azurity Pharmaceuticals, Inc.
- NDC 60631-040 Edarbi · Azilsartan Kamedoxomil 40 mg/1 · Azurity Pharmaceuticals, Inc.