Drug recall D-1233-2020
Product
Levetiracetam Tablets USP 750 mg 120-count bottles, Rx Only, Distributed by: Aurobindo Pharma USA, Inc. 279 Princeton-Hightstown Road East Windsor, NJ 08520, NDC 65862-247-08
Reason for recall
CGMP Deviations: Products were manufactured in a processing area in which water leakage was observed
Lots and codes
Lot #: 24719001A1, Exp. Date 03/2021
Recall details
- Recalling firm
- Aurobindo Pharma USA Inc., East Windsor, NJ
- Quantity
- 8040 units
- Distribution
- Nationwide within the United States
- Type
- Voluntary: Firm initiated
- Recall initiated
- March 18, 2020
- Terminated
- March 25, 2024
Related products
- Levetiracetam – drug information
- NDC 65862-246 Levetiracetam · Levetiracetam 500 mg/1 · Aurobindo Pharma Limited
- NDC 65862-315 Levetiracetam · Levetiracetam 1000 mg/1 · Aurobindo Pharma Limited
- NDC 65862-247 Levetiracetam · Levetiracetam 750 mg/1 · Aurobindo Pharma Limited
- NDC 65862-245 Levetiracetam · Levetiracetam 250 mg/1 · Aurobindo Pharma Limited