Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate And Amphetamine Sulfate Capsule, Extended Release
Product Images NDC 0527-0791

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate And Amphetamine Sulfate (NDC 0527-0791). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lannett Company, 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.

FDA Label Image

Figure (Dextroamphetamine Saccharate Amphetamine Aspartate 1)

A line graph showing mean plasma concentrations of dextroamphetamine and levoamphetamine (ng/mL) over 24 hours. It compares extended-release capsules (20 mg once daily) and tablets (10 mg twice daily) for both dextroamphetamine and levoamphetamine, with separate lines for each formulation. The x-axis represents time in hours; the y-axis shows drug concentration levels.*

FDA Label Image

Label (Dextroamphetamine Saccharate Amphetamine Aspartate 2)

Label for Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate extended-release capsules, 5 mg strength. The label shows product information including active ingredients amounts, storage instructions, dispensing guidance, and the Lannett Company, Inc. as the labeler. The package contains 100 capsules with an NDC of 0527-0790-37.*

FDA Label Image

Label (Dextroamphetamine Saccharate Amphetamine Aspartate 3)

Label for Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate Extended-Release Capsules, 10 mg strength. The label shows it contains 100 capsules and is distributed by Lannett Company, Inc. Usage instructions include storage temperature and dispensing guidance. The label also features a barcode and the Lannett logo.*

FDA Label Image

Label (Dextroamphetamine Saccharate Amphetamine Aspartate 4)

Label for Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate extended-release capsules, 15 mg strength. The label includes dosage details, storage conditions, and states the product is distributed by Lannett Company, Inc. It indicates a package count of 100 capsules and shows an NDC barcode.*

FDA Label Image

Label (Dextroamphetamine Saccharate Amphetamine Aspartate 5)

Label for Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate Extended-Release Capsules, 20 mg strength. The label includes dosage details for each extended-release capsule, storage instructions, medication guide information, and the manufacturer, Lannett Company, Inc. The package contains 100 capsules.*

FDA Label Image

Label (Dextroamphetamine Saccharate Amphetamine Aspartate 6)

Label for Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate Extended-Release Capsules 25 mg by Lannett Company, Inc. This Rx-only package contains 100 capsules. The label includes dosage details, storage instructions, barcode, and directs users to the Medication Guide and prescribing information.*

FDA Label Image

Label (Dextroamphetamine Saccharate Amphetamine Aspartate 7)

Label for Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate extended-release capsules, 30 mg strength. The label indicates 100 capsules per container and is distributed by Lannett Company, Inc. It includes storage instructions, a barcode, and dispensing information. The product is a Schedule II controlled substance.*

* 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.