Amlodipine besylate and Atorvastatin calcium tablets recall: Subpotent
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
Why was Amlodipine besylate and Atorvastatin calcium tablets recalled?
Subpotent drug
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot #: a) C401537, Exp 07/2015; b) C401539, Exp 07/2015
- Product
- 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
- Recalling firm
- Dr. Reddy's Laboratories, Inc.
- Distribution
- Nationwide
- Recall date
- June 24, 2015
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)