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On September 9, 2021 the FDA finally faced a court-ordered deadline to review millions of premarket applications (known as PMTAs) from e-cigarette manufacturers to determine whether the products are appropriate for the protection of public health. The move to authorize Vuse Solo comes after the agency denied the applications of nearly a million flavored products

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Faulcon LM, Rudy S, Limpert J, Wang B, Murphy I