Amlodipine besylate and Atorvastatin calcium tablets, 5mg/10mg, packaged in a)30-count bottle (NDC 43598-322-30), b) 90-count bottle (NDC 43598-322-90), Rx Only, Manufactured by Dr. Reddy's Laboratories Limited Bachupally, 500 090 India
Reported: June 24, 2015 Initiated: May 6, 2015 #D-1143-2015
Product Description
Amlodipine besylate and Atorvastatin calcium tablets, 5mg/10mg, packaged in a)30-count bottle (NDC 43598-322-30), b) 90-count bottle (NDC 43598-322-90), Rx Only, Manufactured by Dr. Reddy's Laboratories Limited Bachupally, 500 090 India
Reason for Recall
Subpotent drug
Details
- Recalling Firm
- Dr. Reddy's Laboratories, Inc.
- Distribution
- Nationwide
- Location
- Princeton, NJ
Frequently Asked Questions
What product was recalled? ▼
Amlodipine besylate and Atorvastatin calcium tablets, 5mg/10mg, packaged in a)30-count bottle (NDC 43598-322-30), b) 90-count bottle (NDC 43598-322-90), Rx Only, Manufactured by Dr. Reddy's Laboratories Limited Bachupally, 500 090 India. Recalled by Dr. Reddy's Laboratories, Inc..
Why was this product recalled? ▼
Subpotent drug
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on June 24, 2015. Severity: Low. Recall number: D-1143-2015.
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