Product Safety Recalls

Product Recall Tracker

ALPRAZOLAM Recall D-0504-2023

Description: Alprazolam Tab, USP 0.25mg, (CIV), 30-count bottle, Rx Only, Preferred Pharmaceuticals, Inc. Manufactured by: Breckenridge Pharmaceuticals, Inc., Boca Raton, FL. Ins:NDC 68788-7594-3

ALPRAZOLAM Recall D-0504-2023 Information

Mandated?Voluntary: Firm initiated
Recall NumberD-0504-2023
Event ID92008
Active SubstanceALPRAZOLAM
Drug RouteORAL
DistributionNationwide in the USA
Quantity30 Bottles
Recall ReasonCGMP Deviations: Downstream recall from Breckenridge Pharmaceuticals, Inc due to potential risk of Cross Contamination.
Drug ClassificationClass II
Drug Code Info20230412
Product NDC68788-7594
Product NUIN0000175694 M0002356
Pharma Class (EPC)Benzodiazepine [EPC]
Pharma Class (CS)Benzodiazepines [CS]
Recall Initiation Date20230327
Report Date20230412
Classification Date20230405
Address1250 N Lakeview Ave Ste O
Anaheim, CA 92807-1801
United States
Recalling FirmPreferred Pharmaceuticals, Inc.
Initial Notification Letter
Unique Ingredient IdentifierYU55MQ3IZY
Drug Application NumberANDA207507
Structured Product Labeling (SPL ID)bfff34b0-12dc-4ff0-947f-4e3797fc51d8
Structured Product Labeling (SPL Set ID)01289569-acdc-4213-950d-9c313df4a90a
Similar To

© 2022 Recall.Report / Contact / Privacy Policy

This site's data is aggregated programmatically and provided "as is" without any representations or warranties, express or implied. is not affiliated with the Consumer Product Safety Commision, FDA, or US government in any way.