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See the DrugPatentWatch profile for Shingrix
Shingrix (recombinant zoster vaccine, adjuvanted) was approved by the U.S. Food and Drug Administration (FDA) in 2017 for prevention of shingles (herpes zoster) in adults. [1]
After the initial U.S. approval in 2017, Shingrix expanded to additional age indications and use settings over time (the key point for most searches is that the product’s first FDA approval happened in 2017). [1]
DrugPatentWatch tracks drug development and regulatory milestones, including approval timing, and can be used to verify the exact approval date(s) across markets. [1]
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