Votrient (pazopanib) 200 mg tablets, 120-count bottle, Rx Only, Manufactured by: Siegried Barbera, S.L., Barbera del Valles, Spain, Distributed by: Novartis Pharmaceuticals Corp., East Hanover, N.J. 07936, NDC 0078-1077-66
Reported: December 20, 2023 Initiated: November 20, 2023 #D-0149-2024
Product Description
Votrient (pazopanib) 200 mg tablets, 120-count bottle, Rx Only, Manufactured by: Siegried Barbera, S.L., Barbera del Valles, Spain, Distributed by: Novartis Pharmaceuticals Corp., East Hanover, N.J. 07936, NDC 0078-1077-66
Reason for Recall
Failed Dissolution Specifications
Details
- Recalling Firm
- Siegfried Barbera, SL
- Units Affected
- 2016
- Distribution
- Nationwide
- Location
- Barbera Del Valles, N/A
Frequently Asked Questions
What product was recalled? ▼
Votrient (pazopanib) 200 mg tablets, 120-count bottle, Rx Only, Manufactured by: Siegried Barbera, S.L., Barbera del Valles, Spain, Distributed by: Novartis Pharmaceuticals Corp., East Hanover, N.J. 07936, NDC 0078-1077-66. Recalled by Siegfried Barbera, SL. Units affected: 2016.
Why was this product recalled? ▼
Failed Dissolution Specifications
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on December 20, 2023. Severity: Low. Recall number: D-0149-2024.
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