Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate And Amphetamine Sulfate Capsule
Product Images NDC 0115-1486

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 0115-1486). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal Pharmaceuticals Of New York 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

E (Dextroamphetamine 1)

A line graph comparing mean plasma concentrations of dextroamphetamine and levoamphetamine over 24 hours after dose administration. The X-axis shows time in hours, and the Y-axis shows concentration in ng/mL. Four different treatments are plotted: extended-release capsules of four combined amphetamine salts (20 mg once daily), ADDERAL tablets (10 mg twice daily) for both dextroamphetamine and levoamphetamine.*

FDA Label Image

1 (Dextroamphetamine 2)

Label for Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate extended-release capsules 5 mg from Amneal Pharmaceuticals of New York LLC. The label indicates 100 capsules, with dosage details and storage instructions. Includes a barcode, QR code, and safety warnings to keep out of children and not use if seal is broken.*

FDA Label Image

1 (Dextroamphetamine 3)

Label for Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate extended-release capsules 10 mg by Amneal Pharmaceuticals. The label includes dosage strength, drug composition details, 100 capsules count, pharmacist instructions, storage information, and a barcode. It also displays the NDC 0115-1487-01 and a QR code linking to the medication guide.*

FDA Label Image

1 (Dextroamphetamine 4)

Label for extended-release capsules of Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate, 15 mg strength, manufactured by Amneal Pharmaceuticals of New York LLC. The label includes directions for pharmacists to dispense a Medication Guide, a count of 100 capsules, storage instructions, and a QR code for accessing the medication guide online.*

FDA Label Image

1 (Dextroamphetamine 5)

Label for Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate extended-release capsules, 20 mg strength, manufactured by Amneal Pharmaceuticals of New York LLC. The label includes drug name, dosage form, strength, quantity of 100 capsules, NDC number 0115-1489-01, storage instructions, and a barcode.*

FDA Label Image

1 (Dextroamphetamine 6)

Label for Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate extended-release capsules, 25 mg strength. The label includes the NDC 0115-1490-01, indicates a 100-capsule count, and shows the Amneal Pharmaceuticals logo. It notes storage instructions and safety warnings, such as keeping out of reach of children and inspection of the safety seal. The label is distributed by Amneal Pharmaceuticals LLC, Bridgewater, NJ.*

FDA Label Image

1 (Dextroamphetamine 7)

Label for Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate extended-release capsules, 30 mg strength. The label includes directions for pharmacists, storage conditions, a barcode, and the labeler, Amneal Pharmaceuticals LLC. The package contains 100 capsules.*

* 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.