Dr. Reddy's Laboratories, Inc. recalls Amlodipine besylate and Atorvastatin calcium tablets, 5mg/10mg, packaged in a)30-count bottle (NDC 43598-322-30), b)
Subpotent drug
Recall notice
Subpotent drug
Contact the company & request your remedy
We’re still writing up this recall
We break every recall down into plain English — this one’s still on our list. Until our write-up is ready, the official FDA hazard and remedy below have the full, accurate details.
Source Page by GovInfoNow · govinfonow.com/recall/44712-dr-reddy-s-laboratories-inc-recalls-amlodipine-besylate-and-atorvastatin · Recall date May 6, 2015 · FDA enforcement record: FDA #D-1143-2015
Cite this page
“Dr. Reddy's Laboratories, Inc. recalls Amlodipine besylate and Atorvastatin calcium tablets, 5mg/10mg, packaged in a)30-count bottle (NDC 43598-322-30), b).” GovInfoNow, recall dated May 6, 2015. https://govinfonow.com/recall/44712-dr-reddy-s-laboratories-inc-recalls-amlodipine-besylate-and-atorvastatin. Based on FDA recall #D-1143-2015 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1143-2015%22&limit=1).
How to tell if you have this one
- Brand
Dr. Reddy's Laboratories, Inc.- Category
Drug
All 4 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class III- Status
Terminated- Distribution
Nationwide- NDC
43598-323-30, 43598-323-60, 43598-323-90, 43598-323-05, 43598-320-30, 43598-320-60, 43598-320-90, 43598-320-05, 43598-317-30, 43598-317-60, 43598-317-90, 43598-317-05, 43598-322-30, 43598-322-60, 43598-322-90, 43598-322-05, 43598-319-30, 43598-319-60, 43598-319-90, 43598-319-05, 43598-316-30, 43598-316-60, 43598-316-90, 43598-316-05, 43598-314-30, 43598-314-60, 43598-314-90, 43598-314-05, 43598-321-30, 43598-321-60, 43598-321-90, 43598-321-05, 43598-318-30, 43598-318-60, 43598-318-90, 43598-318-05, 43598-315-30, 43598-315-60, 43598-315-90, 43598-315-05, 43598-313-30, 43598-313-60, 43598-313-90, 43598-313-05
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| D-1143-2015 | 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; Lot #: a) C401536, Exp 07/2015; b) C401538, Exp 07/2015 | — |
| D-1144-2015 | 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; Lot #: a) C401537, Exp 07/2015; b) C401539, Exp 07/2015 | — |
| D-1145-2015 | Amlodipine besylate and Atorvastatin calcium tablets, 10mg/40mg, 90-count bottle, Rx Only Manufactured by Dr. Reddy's Laboratories Limited Bachupally, 500 090 India, NDC 43598-315-90; Lot # C309280 | — |
| D-1146-2015 | Amlodipine besylate and Atorvastatin calcium tablets, 5mg/40mg packaged in a)30-count bottle (NDC 43598-316-30), b) 90-count bottle (NDC 43598-316-90), Rx Only, Manufactured by Dr. Reddy's Laboratories Limited Bachupally, 500 090 India; Lot # C402439 | — |
Contact Dr. Reddy's Laboratories, Inc.
We’ve drafted a message you can send Dr. Reddy's Laboratories, Inc. to request your refund or repair — edit it as you like.
Subject: Recall D-1143-2015 — Dr. Reddy's Laboratories, Inc. Dr. Reddy's Laboratories, Inc. recalls Amlodipine besylate and Atorv Hello, I own a Dr. Reddy's Laboratories, Inc. recalls Amlodipine besylate and Atorvastatin calcium tablets, 5mg/10mg, packaged in a)30-count bottle (NDC 43598-322-30), b) that is covered by recall D-1143-2015 from Dr. Reddy's Laboratories, Inc.. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Similar recalls
Keep exploring
From people who’ve dealt with this
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-1143-2015 (May 6, 2015) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1143-2015 to see it in context.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
