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Recall Observatory FDA recall evidence

Drug product

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

D-1146-2015

May 06, 2015

Class III

Product summary

Firm
Dr. Reddy's Laboratories, Inc.
Event
Event 71375
Status
Terminated
Classification
Class III
Quantity
Unavailable
Official record key
drug-enforcement:D-1146-2015

Official wording

Reason: Subpotent drug

Code information: Lot # C402439

Distribution pattern: Nationwide

Derived failure modes

  • Potency or specification failure

    reason.potency_specification_failure · v1.0.0

    Subpotent