The U.S. Food and Drug Administration (FDA) is the government agency that regulates marketed drug products and approves marketing of new drug products. The FDA defines a drug product as a finished dosage form (e.g., tablet, capsule, or solution) that contains the drug (called the
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[column]The U.S. Food and Drug Administration has approved Pomalyst (pomalidomide) to treat patients with multiple myeloma whose disease progressed after
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