Class III
Terminated
Lamivudine Tablets, USP, 150 mg, 30 (3x10) count Unit Dose Blisters Carton, NDC 60687-362-21 (Individual Dose NDC: 60687-362-11), Distributed by American Health Packaging, Columbus, OH
This recall has been terminated (originally issued September 18, 2019).
- Company
- American Health Packaging
- Recall Initiated
- August 27, 2019
- Posted
- September 18, 2019
- Recall Number
- D-1847-2019
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 60 cartons
- Firm Location
- Columbus, OH, United States
- Official Source
- View on FDA website ↗
Reason for Recall
Labeling: Incorrect or Missing Package Insert; an error in the Dosage Forms and Strengths section of the insert that incorrectly lists the tablet description coding for the tablets.
Distribution
Nationwide
Lot / Code Info
Lots 186509 and 186982, exp 6/30/2021
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