Dextroamphetamine Saccharate Amphetamine Aspartate Dextroamphetamine Sulfate and Amphetamine Sulfate Amphetamine aspartate 7.5 MG Amphetamine Sulfate 7.5 MG Dextroamphetamine saccharate 7.5 MG Dextroamphetamine Sulfate 7.5 MG Oral Tablet
INDICATIONS AND USAGE Dextroamphetamine saccharate, amphetamine aspartate, dextroamphetamine sulfate and amphetamine sulfate tablets areindicated 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 areindicated 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 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 arefor extended periods should periodically re-evaluate the long-term usefulness of the drug for the individual patient.
Actavis Pharma, Inc.
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HOW SUPPLIED Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets are supplied as follows: 5 mg - Light blue, round, flat-faced beveled edge tablet debossed with ' ' over ‘21’ on one side and four partial scores on the other side. They are available in bottles of 100 tablets (NDC 45963-743-11) with a child-resistant closure. 10 mg - Light blue, round tablet debossed with ' ' over ‘23’ on one side; and scored and partial scored on the other side. They are available in bottles of 100 tablets (NDC 45963-745-11) with a child-resistant closure. 20 mg - peach, round tablet debossed with ' ' over ‘26’ on one side; and scored and partial scored on the other side. They are available in bottles of 100 tablets (NDC 45963-748-11) with a child-resistant closure. 30 mg - peach, round, flat-faced beveled edge tablet debossed with ' ' over ‘28’ on one side; and scored and partial scored on the other side. They are available in bottles of 100 tablets (NDC 45963-749-11) with a child-resistant closure. Store at 20°C to 25°C (68°F to 77°F); excursions permitted to 15°C to 30°C (59°F to 86°F) [See USP Controlled Room Temperature]. Protect from moisture. Dispense in a tight, light-resistant container as defined in the USP. KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN. Brands listed are trademarks of their respective owners. Manufactured by: Actavis Elizabeth LLC 200 Elmora Avenue Elizabeth, NJ 07207 USA Distributed by: Actavis Inc. 60 Columbia Rd., Bldg. B Morristown, NJ 07960 USA 40-9239 Revised - February 2015 actavisimprint5mg actavisimprint10mg actavisimprint20mg actavisimprint30mg
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