Drug recall D-0844-2022
Product
alprazolam XR extended-release tablets, 3 mg, 60-count bottle, Rx only, Distributed by: Greenstone LLC, Peapack, NJ 07977, NDC 59762-0068-1.
Reason for recall
Failed Dissolution Specifications: low out-of-specification dissolution test results observed.
Lots and codes
Lot # EH8348, exp. date August 2023
Recall details
- Recalling firm
- Viatris Inc, Canonsburg, PA
- Quantity
- 6,789 bottles
- Distribution
- Product was distributed nationwide in the USA
- Type
- Voluntary: Firm initiated
- Recall initiated
- April 28, 2022
- Terminated
- June 21, 2023
Related products
- Alprazolam – drug information
- NDC 59762-0066 Alprazolam XR · Alprazolam 2 mg/1 · Mylan Pharmaceuticals Inc.
- NDC 59762-0059 Alprazolam XR · Alprazolam 1 mg/1 · Mylan Pharmaceuticals Inc.
- NDC 59762-0068 Alprazolam XR · Alprazolam 3 mg/1 · Mylan Pharmaceuticals Inc.
- NDC 59762-0057 Alprazolam XR · Alprazolam .5 mg/1 · Mylan Pharmaceuticals Inc.