Product Safety Recalls

Product Recall Tracker

AMOXICILLIN Recall D-1025-2022

Description: Amoxicillin Capsules, USP, 500 mg, 100-count bottle, Rx only, MFG: Sandoz Pharma, NDC 0781-2613-01

AMOXICILLIN Recall D-1025-2022 Information

Mandated?Voluntary: Firm initiated
Recall NumberD-1025-2022
Event ID89646
Original Package?1
Active SubstanceAMOXICILLIN
Drug RouteORAL
DistributionUSA nationwide.
Quantity12 bottles
Recall ReasoncGMP deviations: Temperature abuse
Drug ClassificationClass II
Drug Code Info20220615
Product NDC0781-2020 0781-2613 0781-5060
Drug UPC0307812613016 0307812020012 0307815060015
Recall Initiation Date20220413
Report Date20220615
Classification Date20220609
Address9954 Maryland DriveDeep Run Iii Ste. 4000
Richmond, VA 23233
United States
Recalling FirmMckesson Medical-Surgical Inc. Corporate Office
Initial Notification Letter
Unique Ingredient Identifier804826J2HU
Drug Application NumberANDA064076
Structured Product Labeling (SPL ID)f314ad63-2023-476e-a211-f9cef3be8e2c
Structured Product Labeling (SPL Set ID)13bd4214-9b7f-425b-af5f-fc1ddc678230
Similar To

© 2021 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.