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It can also be applied topically to wounds

Injectable use lacks the same regulatory approval but draws on the same safety mechanisms

(In this scenario, the applicable percent reduction would be 50 percent for the second applicable period for a generic Part D rebatable drug or plasma-derived product and 10 percent for a Part D rebatable drug that is not a generic drug or plasma-derived product.) When the status of a Part D rebatable drug changes from currently in shortage to resolved and either remains in the status of resolved or is removed from the list for at least one applicable period, and then subsequently reemerges on a shortage list, the subsequent shortage will be treated as a new shortage