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valsartan blood pressure drug recall widens - Valsartan Blood Pressure Drug Recall Widens

Valsartan Blood Pressure Drug Recall Widens

Valsartan Blood Pressure Drug Recall Widens

Dec. 7, 2018 — Drugmaker Mylan Pharmaceuticals this week introduced it has expanded its earlier recall of valsartan-based blood force drugs to incorporate all present plenty of the drug that experience now not expired.

The growth contains an extra 104 rather a lot:

26 plenty of Amlodipine and Valsartan Tablets, in five mg/160 mg, 10 mg/160 mg, five mg/320 mg, and 10 mg/320 mg strengths.

51 plenty of Valsartan Tablets in 40 mg, 80 mg, 160 mg, and 320 mg strengths.

27 plenty of Valsartan and Hydrochlorothiazide Tablets, USP (80 mg/12.five mg, 160 mg/12.five mg, 160 mg/25 mg, 320 mg/12.five mg and 320 mg/25 mg strengths).

The medication have been recalled on account of hint quantities of an impurity, N-nitrosodiethylamine, or NDEA, which might motive most cancers in people, in step with the International Agency for Research on Cancer.

The newest recall joins many others of new weeks, all of which have been made, or come with components made, in China or India.

You can discover a complete record of all recalled valsartan merchandise right here.



Sources

FDA.gov: “Mylan Expands Its Voluntary Nationwide Recall of Valsartan Tablets, USP, Amlodipine and Valsartan Tablets, USP, and Valsartan and Hydrochlorothiazide Tablets, USP, to all Lots Within Expiry Due to The Detection of Trace Amounts of NDEA (N-Nitrosodiethylamine) Impurity Found in the Active Pharmaceutical Ingredient.”



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