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U.S. Department of Health and Human Services

Enforcement Report - Week of June 24, 2015

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Product Detail

Product Description Amlodipine besylate and Atorvastatin calcium tablets, 10mg/10mg, packaged in a)30-count bottle (NDC 43598-321-30), b) 90-count bottle (NDC 43598-321-90), Rx Only, Manufactured by Dr. Reddy's Laboratories Limited Bachupally, 500 090 India
Recall Number D-1144-2015
Classification Class III
Code Info Lot #: a) C401537, Exp 07/2015; b) C401539, Exp 07/2015
Product Distributed Qty
Reason For Recall Subpotent drug

Event Detail

Event Id 71375
Product Type Drugs
Status Ongoing
Recalling Firm Dr. Reddy's Laboratories, Inc.
City Princeton
State NJ
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2015-05-06
Initial Firm Notification of Consignee or Public Letter
Distribution Pattern Nationwide
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