Oxybutynin Chloride, Extended-Release Tablets USP, 10 mg, 100 Tablet, Rx Only, Distributed by: Lannett Company, Inc, Philadelphia, PA 19154 NDC: 62175-271-37
Reported: March 20, 2019 Initiated: February 21, 2019 #D-0996-2019
Product Description
Oxybutynin Chloride, Extended-Release Tablets USP, 10 mg, 100 Tablet, Rx Only, Distributed by: Lannett Company, Inc, Philadelphia, PA 19154 NDC: 62175-271-37
Reason for Recall
Failed Dissolution Specifications
Details
- Recalling Firm
- Lannett Company Inc.
- Units Affected
- 14,448 bottles
- Distribution
- Nationwide, including Puerto Rico.
- Location
- Seymour, IN
Frequently Asked Questions
What product was recalled? ▼
Oxybutynin Chloride, Extended-Release Tablets USP, 10 mg, 100 Tablet, Rx Only, Distributed by: Lannett Company, Inc, Philadelphia, PA 19154 NDC: 62175-271-37. Recalled by Lannett Company Inc.. Units affected: 14,448 bottles.
Why was this product recalled? ▼
Failed Dissolution Specifications
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on March 20, 2019. Severity: Low. Recall number: D-0996-2019.
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