Recalling firm
Dr. Reddy's Laboratories, Inc.
Product type
Drug
Status
Terminated
Report date
2024-07-10
Distribution
IL, MS, OH
Firm state
NJ
Product quantity
20,520 units
Initiated by
Voluntary: Firm initiated
Reason for recall
Presence of foreign substance.
Product description
Allopurinol Tablets, USP 300mg, 100 Tablets per bottle, Rx only, Manufactured By: Dr. Reddy's Laboratories LA LLC, Shreveport, LA 71106 USA, NDC 55111-730-01.
Code / lot info
L2300594
Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.