The information in this section can help you work with your health professionals to make the best medicine choices, buy safely, and use medicine so it’s as safe and effective as possible.
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Task Description Request Please post to the OII FOIA Electronic Reading Room
Record Date 02/20/2025
Short Title (70 char) BlendHouse Allerton LLC. Allerton, PA. 483 issued 02/20/2025
FEI Number 1921383
Firm Name BlendHouse Allerton LLC
Record Type 483
State PA
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Section 807 of the FDA Reauthorization Act of 2017 (FDARA) requires the FDA to report on certain abbreviated new drug applications (ANDAs).National Drug Code Directory
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This communication is part of the Communications Pilot to Enhance the Medical Device Recall Program.