Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, Amphetamine Sulfate Tablet
Product Images NDC 68462-652

Each tablet contains 7.5 mg of dextroamphetamine saccharate, 7.5 mg of amphetamine aspartate monohydrate, 7.5 mg of dextroamphetamine sulfate, and 7.5 mg of amphetamine sulfate, with a total amphetamine base equivalence of 18.8 mg. The usual dosage should be followed as per package insert. Store between 20°C-25°C (68°F-77°F). Dispense in a tight, light-resistant container with a child-resistant closure. Keep out of reach of children. Manufactured by Neolpharma, Inc., Caguas, Puerto Rico, distributed by Glenmark Pharmaceuticals Inc., USA. This is a single entity amphetamine product combining various salts. The pharmacist must dispense the medication guide provided separately to each patient. The product comes in a bottle of 100 tablets. Additional information and medication guide can be found at the Glenmark Pharmaceuticals website.*

This text describes a medication containing dextroamphetamine saccharate, amphetamine aspartate, dextroamphetamine sulfate, and amphetamine sulfate. The tablets are used to administer a total of 3 mg of total amphetamine base equivalence. The usual dosage guidance can be found in the package insert. The medication should be stored at 20°C to 25°C (68°F to 77°F) in a controlled room temperature. It is advised to keep the medication out of the reach of children and dispense it in a light-resistant container with a child-resistant closure. The medication is manufactured by Neolpharma, Inc. in Puerto Rico and distributed by Glenmark Pharmaceuticals Inc. in the USA. The prescription details include the National Drug Code (NDC) number, lot number, and expiration date. A medication guide should be provided separately to each patient by the pharmacist. The medication comes in a container containing 100 tablets.*

This text provides information on a medication in tablet form containing different forms of amphetamine, such as dextroamphetamine saccharate, amphetamine aspartate, dextroamphetamine sulfate, and amphetamine sulfate. It includes details on storage conditions, child-resistant packaging, manufacturer, distributor, prescribing information, controlled room temperature, and guidelines for dispensing by pharmacists. The medication is available in a pack of 100 tablets with a specific NDC (National Drug Code) number. More information can be found in the package insert or medication guide provided separately to each patient.*

Each tablet in this medication contains a combination of 5 mg of dextroamphetamine saccharate, 5 mg of amphetamine aspartate monohydrate, 5 mg of dextroamphetamine sulfate, USP and Dextroamphetamine saccharate. It is recommended to store this medication in a tight, light-resistant container with a child-resistant closure and to keep it out of the reach of children. The medication is manufactured by Neolpharma, Inc. in Caguas, Puerto Rico, and distributed by Glenmark Pharmaceuticals Inc. in Mahwah, NJ. The medication guide can be obtained online at www.glenmarkpharma-us.com/medguides.*

This text describes a medication in tablet form that contains dextroamphetamine saccharate, amphetamine aspartate monohydrate, dextroamphetamine sulfate, and amphetamine sulfate. The tablets are to be stored at room temperature in a light-resistant container with a child-resistant closure. The medication is manufactured by Neolpharma, Inc. and distributed by Glenmark Pharmaceuticals Inc. The text also mentions a medication guide available online and provides information about distribution and lot number.*

Not available.*