Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate And Amphetamine Sulfate Tablet
Product Images NDC 0527-0766

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate And Amphetamine Sulfate (NDC 0527-0766). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lannett Company, Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Label (Dextroamphetamine Saccharate Amphetamine Aspartate 1)

Label for Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets, 5 mg strength. The label indicates it contains 100 tablets and is distributed by Lannett Company, Inc. It includes dosage instructions, storage info, and a barcode. The label cautions to keep medication out of reach of children and to refer to the medication guide.*

FDA Label Image

Label (Dextroamphetamine Saccharate Amphetamine Aspartate 2)

Label for Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets, 7.5 mg strength. The label includes dosage information, storage instructions, and a note to keep medication out of children's reach. The product is distributed by Lannett Company, Inc. and comes in a bottle of 100 tablets.*

FDA Label Image

Label (Dextroamphetamine Saccharate Amphetamine Aspartate 3)

Label for Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets 10 mg by Lannett Company, Inc. The label states each tablet contains 2.5 mg of each active component (4 total) equaling 6.3 mg amphetamine base equivalent. The package contains 100 oral tablets with prescription only status. Storage instructions and a barcode are also visible.*

FDA Label Image

Label (Dextroamphetamine Saccharate Amphetamine Aspartate 4)

Label for Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets, 12.5 mg strength. The label includes instructions about dosage, storage conditions, and keeping medication out of reach of children. It indicates prescription use only, contains 100 tablets, and is labeled by Lannett Company, Inc. The label features dosage and medication guides information and a barcode.*

FDA Label Image

Label (Dextroamphetamine Saccharate Amphetamine Aspartate 5)

Label for Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets, 15 mg strength, oral tablet dosage form. The label states these are mixed salts of a single-entity amphetamine product, supplied by Lannett Company, Inc. It includes dosage information, storage instructions, a barcode, and that the package contains 100 tablets for prescription use only.*

FDA Label Image

Label (Dextroamphetamine Saccharate Amphetamine Aspartate 6)

Label for Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets 20 mg by Lannett Company, Inc. The label indicates each tablet contains 5 mg of each listed amphetamine salt, totaling 20 mg. The package contains 100 tablets. Directions on storage and dosage guidance references are included, as well as a barcode and distributor address.*

FDA Label Image

Label (Dextroamphetamine Saccharate Amphetamine Aspartate 7)

Packaging label for Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate tablets, 30 mg strength. The label indicates the product contains mixed salts of a single-entity amphetamine product, supplied by Lannett Company, Inc. The package contains 100 tablets with storage instructions and dosing guidance noted.*

* 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.