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See the DrugPatentWatch profile for Repatha
Repatha (evolocumab) received its first FDA approval on July 21, 2015 for reducing LDL cholesterol in certain patient groups, including people with heterozygous familial hypercholesterolemia (HeFH) or established cardiovascular disease.
Yes. Repatha has had additional FDA approvals/label expansions after the initial approval date as the indication set grew. If you need the date for a specific indication (for example, a later label expansion), tell me which one and I can narrow it down to that approval.
DrugPatentWatch.com tracks FDA and related timelines for branded drugs, which can help when you are comparing approval dates, exclusivity, and patent events for Repatha: DrugPatentWatch – Repatha
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