dextroamphetamine saccharate amphetamine aspartate dextroamphetamine sulfate and amphetamine sulfate 10 mg
INDICATIONS AND USAGE Dextroamphetamine saccharate, amphetamine aspartate, dextroamphetamine sulfate, and amphetamine sulfate tablets are indicated for the treatment of Attention Deficit Hyperactivity Disorder (ADHD) and Narcolepsy. Attention Deficit Hyperactivity Disorder (ADHD) A diagnosis of Attention Deficit Hyperactivity Disorder (ADHD; DSM-IV ® ) implies the presence of hyperactive-impulsive or inattentive symptoms that caused impairment and were present before age 7 years. The symptoms must cause clinically significant impairment, e.g., in social, academic, or occupational functioning, and be present in two or more settings, e.g., school (or work) and at home. The symptoms must not be better accounted for by another mental disorder. For the Inattentive Type, at least six of the following symptoms must have persisted for at least 6 months: lack of attention to details/careless mistakes; lack of sustained attention; poor listener; failure to follow through on tasks; poor organization; avoids tasks requiring sustained mental effort; loses things; easily distracted; forgetful. For the Hyperactive-Impulsive Type, at least six of the following symptoms must have persisted for at least 6 months: fidgeting/squirming; leaving seat; inappropriate running/climbing; difficulty with quiet activities; “on the go;†excessive talking; blurting answers; can't wait turn; intrusive. The Combined Type requires both inattentive and hyperactive-impulsive criteria to be met. Special Diagnostic Considerations Specific etiology of this syndrome is unknown, and there is no single diagnostic test. Adequate diagnosis requires the use not only of medical but of special psychological, educational, and social resources. Learning may or may not be impaired. The diagnosis must be based upon a complete history and evaluation of the child and not solely on the presence of the required number of DSM-IV ® characteristics. Need for Comprehensive Treatment Program Dextroamphetamine saccharate, amphetamine aspartate, dextroamphetamine sulfate, and amphetamine sulfate tablets are indicated as an integral part of a total treatment program for ADHD that may include other measures (psychological, educational, social) for patients with this syndrome. Drug treatment may not be indicated for all children with this syndrome. Stimulants are not intended for use in the child who exhibits symptoms secondary to environmental factors and/or other primary psychiatric disorders, including psychosis. Appropriate educational placement is essential and psychosocial intervention is often helpful. When remedial measures alone are insufficient, the decision to prescribe stimulant medication will depend upon the physician's assessment of the chronicity and severity of the child's symptoms. Long-Term Use The effectiveness of dextroamphetamine saccharate, amphetamine aspartate, dextroamphetamine sulfate, and amphetamine sulfate tablets for long-term use has not been systematically evaluated in controlled trials. Therefore, the physician who elects to use dextroamphetamine saccharate, amphetamine aspartate, dextroamphetamine sulfate, and amphetamine sulfate tablets for extended periods should periodically reevaluate the long-term usefulness of the drug for the individual patient.
ascent pharmaceuticals, inc
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HOW SUPPLIED
DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE, AND AMPHETAMINE SULFATE tablets is supplied as follows: 5 mg: white to off white round tablets with ‘T370’ debossed on one side and four partial bisects on other side. NDC 43602-370-01 bottles of 100 tablets NDC 43602-370-05 bottles of 500 tablets 7.5 mg: Light blue color oval tablet, one side debossed with ‘T371’ with two partial bisects and other side with two partial bisects and one full bisect. NDC 43602-371-01 bottles of 100 tablets NDC 43602-371-05 bottles of 500 tablets 10 mg: Light blue color round shaped tablet debossed with T over 372 on one side and other side with one full bisect and two partial bisects. NDC 43602-372-01 bottles of 100 tablets NDC 43602-372-05 bottles of 500 tablets 12.5 mg: Light to dark peach colored, round beveled edge tablet, debossed with “T†over “373†on one side and one full bisect and two partial bisects on other side. NDC 43602-373-01 bottles of 100 tablets NDC 43602-373-05 bottles of 500 tablets 15 mg: Light to dark peach colored oval shaped tablet, debossed with ‘T374’ with two partial bisects on one side, and one full bisect and two partial bisects on other side. NDC 43602-374-01 bottles of 100 tablets NDC 43602-374-05 bottles of 500 tablets 20 mg: Light to dark peach colored round tablet, debossed with T over 375 on one side and other side with one full bisect and two partial bisects. NDC 43602-375-01 bottles of 100 tablets NDC 43602-375-05 bottles of 500 tablets 30 mg: Light to dark peach round, flat faced, beveled edge tablets with one full bisect and two partial bisect lines on one side, and debossed with “T†over “376†on other side. NDC 43602-376-01 bottles of 100 tablets NDC 43602-376-05 bottles of 500 tablets Dispense in a tight, light-resistant container. Store at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature]. Manufactured by: Ascent Pharmaceuticals, Inc. Central Islip, NY 11722 Rev: 04/21
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