PHENYTOIN SODIUM Recall D-0090-2024
Description: Extended Phenytoin Sodium Capsules, USP, 100 mg, 100-count bottle, Distributed by Amneal Pharmaceuticals LLC Bridgewater, NJ, 08807, NDC# 65162-212-10
PHENYTOIN SODIUM Recall D-0090-2024 Information
Status | Ongoing |
Mandated? | Voluntary: Firm initiated |
Recall Number | D-0090-2024 |
Event ID | 93292 |
Brand | EXTENDED PHENYTOIN SODIUM |
Generic Name | PHENYTOIN SODIUM |
Manufacturer | PHENYTOIN SODIUM |
Original Package? | 1 |
Active Substance | PHENYTOIN SODIUM |
Drug Route | ORAL |
Distribution | Nationwide in the USA and Puerto Rico |
Quantity | 9,263 100-count bottles |
Recall Reason | Failed Dissolution Specifications |
Drug Classification | Class II |
Drug Code Info | 20231115 |
Product NDC | 65162-212 |
Drug UPC | 0365162212037 0365162212105 |
Recall Initiation Date | 20231027 |
Report Date | 20231115 |
Classification Date | 20231107 |
Address | 50 Horseblock Rd Brookhaven, NY 11719-9509 United States |
Recalling Firm | Amneal Pharmaceuticals of New York, LLC |
Initial Notification | Letter |
Unique Ingredient Identifier | 4182431BJH |
Drug Application Number | ANDA040765 |
Structured Product Labeling (SPL ID) | f629af5d-faef-4416-9b98-55a3a5ec8271 |
Structured Product Labeling (SPL Set ID) | 7e467c02-49a0-4b62-b537-430fdfa4f10e |
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