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Dextroamphetamine Sulfate
Product Images NDC 40032-870
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Dextroamphetamine Sulfate (NDC 40032-870). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Novel Laboratories, Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
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This is a medication guide for Dextroamphetamine Sulfate Tablets. Each tablet contains 5 mg of Dextroamphetamine sulfate, USP, and the usual dosage can be found in the package insert. It is important to use safety closures when dispensing this product unless otherwise directed by a physician. The medication should be stored at 20° to 25°C (68° to 7°} Controlled Room Temperature, and should be dispensed in a tight, light-resistant container with a child-resistant closure. It is important to keep this and all medications out of the reach of children. The manufacturer is Novel Laboratories, Inc., located in Somerset, NJ.*
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This is a prescription drug description for Dextroamphetamine USP sulfate tablets. The text includes the drug's National Drug Code (NDC) number and dosage information. It also includes a recommendation for pharmacists to provide a medication guide to each patient.*
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This is a label of Dextroamphetamine Sulfate Tablets, USP, containing 10mg of the active ingredient per tablet. The tablets are prescription-only and come in a tightly sealed, light-resistant container with a child-resistant closure as required by the USP. The pharmacist is advised to provide patients with a medication guide, and the usual dosage is outlined in the package insert. The product should be stored at controlled room temperature away from children, and safety closures should be used when dispensing, except where ordered by a physician or requested by the purchaser. The label includes the manufacturer's name and location, along with the lot number and revision date.*
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* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.
