The U.S. Food and Drug Administration (FDA) said today that it has made decisions on more than 99 percent of the nearly 26 million considered tobacco products submitted for premarket tobacco product applications (PMTAs). The agency has previously said reviews of some of the most popular vaping products could take until the end of the year.
“These applications are group submissions for e-liquids of different sizes, nicotine strengths, and flavor combinations, and each is considered a separate product application under the existing premarket review process,” the FDA wrote in a statement.
The agency’s overall decision included authorizing 23 new vaping products and devices, and issuing refuse-to-accept (RTA) letters, refuse-to-submit letters, or marketing denial orders for millions of products.
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