:max_bytes(150000):strip_icc()/Health-med-recall-2-87a5dc48f8ad4e71b84a0112890d0cd8.png?w=1920&resize=1920,1280&ssl=1 "FDA Announces Nationwide Recall of Common Blood Pressure Medication—More Than 11,000 Bottles Affected")
A nationwide recall is underway for greater than 11,000 bottles of a typical blood strain remedy, the Meals and Drug Administration (FDA) reported. The medicine—a generic model of Ziac—had been initially recalled on Nov. 21 after pattern testing discovered hint quantities of a ldl cholesterol remedy made by the identical firm, Glenmark Prescription drugs. On Dec. 1, the FDA gave the recall a Class III danger degree, indicating a low danger of hurt.
The recall impacts prescription 2.5-milligram/6.25-milligram bisoprolol fumarate and hydrochlorothiazide tablets within the following sizes and codes:
Measurement
Nationwide Drug Code (NDC)
Lot Codes
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