VISTARIL (hydroxyzine pamoate) by Pfizer is clinical pharmacology hydroxyzine pamoate is unrelated chemically to the phenothiazines, reserpine, meprobamate, or the benzodiazepines. Approved for anxiety. First approved in 1959.
Drug data last refreshed 18h ago · AI intelligence enriched 2w ago
VISTARIL (hydroxyzine pamoate) is an oral anxiolytic suspension approved in 1959 for the treatment of anxiety. It works by suppressing activity in key subcortical regions of the central nervous system and exhibits muscle relaxant, antihistaminic, analgesic, and antiemetic properties. Clinical effects typically appear within 15–30 minutes of oral administration.
Product is in late lifecycle with modest Medicare spending and 206 claims in 2023; brand team likely focused on defending market share against generic and therapeutic alternatives rather than growth initiatives.
CLINICAL PHARMACOLOGY Hydroxyzine pamoate is unrelated chemically to the phenothiazines, reserpine, meprobamate, or the benzodiazepines. Hydroxyzine pamoate is not a cortical depressant, but its action may be due to a suppression of activity in certain key regions of the subcortical area of the…
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The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.
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Upgrade to Pro — $25/moVISTARIL pamoate offers limited career growth potential given its approaching loss of exclusivity and stable but small commercial footprint ($17K Part D spending). Roles available are primarily defensive—managing generic transition, maintaining formulary access, and supporting legacy product lifecycle management rather than building new market share.