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XANAX Tablets contain alprazolam which is a triazolo analog of the 1,4 benzodiazepine class of central nervous system-active compounds.
The chemical name of alprazolam is 8-Chloro-1-methyl-6-phenyl-4H-s-triazolo [4,3-α] [1,4] benzodiazepine.
XANAX Tablet, for oral administration, contains 2 mg of alprazolam.
XANAX Tablets, 2 mg, are multi-scored and may be divided as shown below:
Cellulose, corn starch, docusate sodium, lactose, magnesium stearate, silicon dioxide and sodium benzoate.
XANAX Tablets (alprazolam) are indicated for the management of anxiety disorder (a condition corresponding most closely to the APA Diagnostic and Statistical Manual [DSM-IIIR] diagnosis of generalized anxiety disorder) or the short-term relief of symptoms of anxiety. Anxiety or tension associated with the stress of everyday life usually does not require treatment with an anxiolytic.
Anxiety associated with depression is responsive to XANAX.
Studies supporting this claim were conducted in patients whose diagnoses corresponded closely to the DSM-III-R/IV criteria for panic disorder (see Clinical Studies).
Panic disorder (DSM-IV) is characterized by recurrent unexpected panic attacks, ie, a discrete period of intense fear or discomfort in which four (or more) of the following symptoms develop abruptly and reach a peak within 10 minutes:
(1) palpitations, pounding heart, or accelerated heart rate;
(3) trembling or shaking;
(4) sensations of shortness of breath or smothering;
(5) feeling of choking;
(6) chest pain or discomfort;
(7) nausea or abdominal distress;
(8) feeling dizzy, unsteady, lightheaded, or faint;
(9) derealization (feelings of unreality) or depersonalization (being detached from oneself);
(10) fear of losing control;
(11) fear of dying;
(12) paresthesias (numbness or tingling sensations);
(13) chills or hot flushes.
The physician should periodically reassess the usefulness of the drug for the individual patient.
2 mg (white, oblong, multi-scored, imprinted “XANAX ” on one side and “2” on the reverse side)