24 HR Methylphenidate Hydrochloride 54 MG Extended Release Oral Tablet
1 INDICATIONS AND USAGE Methylphenidate hydrochloride extended-release tablets are indicated for the treatment of Attention Deficit Hyperactivity Disorder (ADHD) in children 6 years of age and older, adolescents, and adults up to the age of 65 [see Clinical Studies ( 14 )] . Methylphenidate hydrochloride extended-release tablets are a CNS stimulant indicated for the treatment of Attention Deficit Hyperactivity Disorder (ADHD) in children 6 years of age and older, adolescents, and adults up to the age of 65. ( 1 )
actavis pharma, inc.
OVAL RED logo 727
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16 HOW SUPPLIED/STORAGE AND HANDLING
METHYLPHENIDATE HYDROCHLORIDE extended-release tablets, USP are available as follows: 18 mg – Each yellow, film-coated, capsule shaped tablet imprinted with the Andrx logo and 725 on one side and plain on the other side contains 18 mg
METHYLPHENIDATE HYDROCHLORIDE, USP. Tablets are supplied in bottles of 100 (NDC 62037-725-01). 27 mg – Each gray, film-coated, capsule shaped tablet imprinted with the Andrx logo and 734 on one side and plain on the other side contains 27 mg
METHYLPHENIDATE HYDROCHLORIDE, USP. Tablets are supplied in bottles of 100 (NDC 62037-734-01). 36 mg – Each white, film-coated, capsule shaped tablet imprinted with the Andrx logo and 726 on one side and plain on the other side contains 36 mg
METHYLPHENIDATE HYDROCHLORIDE, USP. Tablets are supplied in bottles of 100 (NDC 62037-726-01). 54 mg – Each red brown, film-coated, capsule shaped tablet imprinted with the Andrx logo and 727 on one side and plain on the other side contains 54 mg
METHYLPHENIDATE HYDROCHLORIDE, USP. Tablets are supplied in bottles of 100 (NDC 62037-727-01). Storage and Handling Store at 20° to 25°C (68° to 77°F); excursions permitted to 15° to 30°C (59° to 86°F) [See USP Controlled Room Temperature]. Protect from humidity. Dispense in tight, light-resistant container as defined in USP, with a child-resistant closure (as required).
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