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Class III: unlikely to cause harmTerminated

Dr. Reddy's Laboratories Amlodipine besylate and Atorvastatin calcium Recall

Amlodipine besylate and Atorvastatin calcium Tablets,2

Dr. Reddy's Laboratories, Inc. · Princeton, NJ

Risk level
Class III
Reported by FDA
Sep 2, 2015
Recall ID
D-1375-2015
Check your lot numberHow we source this data

Summary

Dr. Reddy's Laboratories recalled Amlodipine besylate and Atorvastatin calcium starting Aug 13, 2015. The FDA classified it as Class III (unlikely to cause harm) and published enforcement report D-1375-2015 on Sep 2, 2015. Reason: Subpotent Drug: Subpotent atorvastatin. Status: Terminated.

Why it was recalled

Subpotent Drug: Subpotent atorvastatin.

Product description

Amlodipine besylate and Atorvastatin calcium Tablets,2.5 mg/40 mg, 30 Count Bottles, Rx Only. Manufactured by Dr. Reddy's Laboratories Limited, Bachupally - 500 090 India. NDC: 43598-317-30.

Lot numbers, UPCs & expiration codes

Lot #: C402341, Expiry: 08/2015

Where it was sold

U.S. Nationwide

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-1375-2015
Classification
Class III
Status
Terminated
Recall initiated
Aug 13, 2015
FDA report date
Sep 2, 2015
Quantity
984 Bottles
Recall type
Voluntary: Firm initiated
Recalling firm
Dr. Reddy's Laboratories, Inc.

Original FDA data

Every field from FDA enforcement report D-1375-2015, exactly as published.

Show all FDA fields
City
Princeton
State
NJ
Status
Terminated
Country
United States
Event ID
71984
Address
107 College Rd E
Code information
Lot #: C402341, Expiry: 08/2015
Postal code
08540-6623
Report date
Sep 2, 2015
Product type
Drugs
Recall number
D-1375-2015
Classification
Class III
Recalling firm
Dr. Reddy's Laboratories, Inc.
Product quantity
984 Bottles
Termination date
Dec 15, 2016
Reason for recall
Subpotent Drug: Subpotent atorvastatin.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Amlodipine besylate and Atorvastatin calcium Tablets,2.5 mg/40 mg, 30 Count Bottles, Rx Only. Manufactured by Dr. Reddy's Laboratories Limited, Bachupally - 500 090 India. NDC: 43598-317-30.
Distribution pattern
U.S. Nationwide
Recall initiation date
Aug 13, 2015
Initial firm notification
Letter
Center classification date
Aug 27, 2015

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1375-2015, published Sep 2, 2015. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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