Amlodipine besylate and Atorvastatin calcium Tablets, 10 mg/20 mg, Packaged in a) 30 Count Bottles (NDC: 43598-318-30) and b) 90 Count Bottles (NDC: 43598-318-90), Rx Only. Manufactured by Dr. Reddy's Laboratories Limited, Bachupally - 500 090 India
Reported: September 2, 2015 Initiated: August 13, 2015 #D-1377-2015
Product Description
Amlodipine besylate and Atorvastatin calcium Tablets, 10 mg/20 mg, Packaged in a) 30 Count Bottles (NDC: 43598-318-30) and b) 90 Count Bottles (NDC: 43598-318-90), Rx Only. Manufactured by Dr. Reddy's Laboratories Limited, Bachupally - 500 090 India
Reason for Recall
Subpotent Drug: Subpotent atorvastatin.
Details
- Recalling Firm
- Dr. Reddy's Laboratories, Inc.
- Units Affected
- a) 16,080 and b) 480 Bottles
- Distribution
- U.S. Nationwide
- Location
- Princeton, NJ
Frequently Asked Questions
What product was recalled? ▼
Amlodipine besylate and Atorvastatin calcium Tablets, 10 mg/20 mg, Packaged in a) 30 Count Bottles (NDC: 43598-318-30) and b) 90 Count Bottles (NDC: 43598-318-90), Rx Only. Manufactured by Dr. Reddy's Laboratories Limited, Bachupally - 500 090 India. Recalled by Dr. Reddy's Laboratories, Inc.. Units affected: a) 16,080 and b) 480 Bottles.
Why was this product recalled? ▼
Subpotent Drug: Subpotent atorvastatin.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on September 2, 2015. Severity: Low. Recall number: D-1377-2015.
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