3070 Release 24 HR Methylphenidate Hydrochloride 10 MG Extended Release Oral Capsule
INDICATION AND USAGE Attention Deficit Hyperactivity Disorder (ADHD) Methylphenidate HCl Extended-Release Capsules CD are indicated for the treatment of Attention Deficit Hyperactivity Disorder (ADHD). The efficacy of Methylphenidate HCl Extended-Release Capsules CD in the treatment of ADHD was established in one controlled trial of children aged 6 to 15 who met DSM-IV criteria for ADHD (see CLINICAL PHARMACOLOGY ). 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 Types 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 Methylphenidate HCl Extended-Release Capsules CD is 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 Methylphenidate HCl Extended-Release Capsules CD for long-term use, i.e., for more than 3 weeks, has not been systematically evaluated in controlled trials. Therefore, the physician who elects to use Methylphenidate HCl Extended-Release Capsules CD for extended periods should periodically re-evaluate the long-term usefulness of the drug for the individual patient (see DOSAGE AND ADMINISTRATION ).
lannett company, inc.
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HOW SUPPLIED Methylphenidate HCl Extended-Release capsules CD are available in six strengths: 10 mg, green/white capsules, imprinted with “LANNETT 4579” in white letters on the green cap, and “10 mg” in black letters on the white body of the capsule. NDC 0527-4579-37 Bottle of 100 capsules 20 mg, blue/white capsules, imprinted with “LANNETT 4580” in white letters on the blue cap, and “20 mg” in black letters on the white body of the capsule. NDC 0527-4580-37 Bottle of 100 capsules 30 mg, reddish-brown/white capsules, imprinted with “LANNETT 4581” in white letters on the reddish-brown cap, and “30 mg” in black letters on the white body of the capsule. NDC 0527-4581-37 Bottle of 100 capsules 40 mg, yellow ivory/white capsules, imprinted with “LANNETT 4582” in black letters on the yellow ivory cap, and “40 mg” in black letters on the white body of the capsule. NDC 0527-4582-37 Bottle of 100 capsules 50 mg, purple/white capsules, imprinted with “LANNETT 4583” in white letters on the purple cap, and “50 mg” in black letters on the white body of the capsule. NDC 0527-4583-37 Bottle of 100 capsules 60 mg, white/white capsules, imprinted with “LANNETT 4584” in black letters on the white cap, and “60 mg” in black letters on the white body of the capsule. NDC 0527-4584-37 Bottle of 100 capsules Store at 25°C (77°F); excursions permitted to 15°-30°C (59°-86°F) [See USP Controlled Room Temperature]. Keep out of the reach of children.
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