Reported Mar 11, 2015 · Terminated
AMLODIPINE BESYLATE TABLETS USP, 10 mg*, 1000 count bottles (NDC 0603-2110-32), Rx only, Manufactured for: QUALITEST…
Qualitest Pharmaceuticals
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Qualitest Pharmaceuticals · 120 Vintage Dr NE · Huntsville, AL · 35811-8216
Is this the product you have?
- AMLODIPINE BESYLATE TABLETS USP, 10 mg*, 1000 count bottles (NDC 0603-2110-32), Rx only
- Manufactured forQUALITEST PHARMACEUTICALS, HUNTSVILLE, AL 35811
- Lot codes and dates
Lot T018H14AExp 08/16
- Amount recalled
- 2808 bottles
Where it was sold
- Nationwide
Why it was recalled
Failed tablet specifications: One lot was found to contain oversized tablets.
This product could cause temporary or reversible health problems — stop using it.
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