Drug Enforcement D-0047-2025

Failed Tablet/Capsule Specifications

Status

Ongoing

Classification

Class III

Report Date

November 27, 2024

Termination Date

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Product Information

Product description
IBU (ibuprofen) 600 mg tablets, 500-count bottle, Rx Only, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made in India, NDC 55111-683-05
Product quantity
3416 botttles
Reason for recall
Failed Tablet/Capsule Specifications
Recall initiation reason
—
Initial firm notification
N/A
Distribution pattern
USA Nationwide

Location & Firm

Recalling firm
Dr. Reddy's Laboratories, Inc.
Address
107 College Rd E, N/A

United States
Voluntary / Mandated
Voluntary: Firm initiated
Status date
—

Codes & Dates

Recall number
D-0047-2025
Event ID
95620
Recall initiation date
October 29, 2024
Center classification date
November 15, 2024
Code info
Lot #: C5406201, Exp 03/31/2028
More code info
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