Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate And Amphetamine Sulfate Capsule, Extended Release
Product Images NDC 63629-1974

2 FDA label images from Bryant Ranch Prepack · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate And Amphetamine Sulfate (NDC 63629-1974). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

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

Product Images & Figures Index

FDA Label Image

Figure-1 (Image 01)

Figure-1 (Image 01)
A line graph showing mean plasma concentrations of dextroamphetamine and levoamphetamine over 24 hours. It compares extended-release capsules 20 mg once daily and tablets 10 mg twice daily formulations of Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, and Amphetamine Sulfate. The x-axis represents time in hours, and the y-axis shows concentration in ng/mL.*
FDA Label Image

Label (Lbl636291974)

Label (Lbl636291974)
The label details the contents of each extended-release capsule of Dextroamphetamine Sulf-Saccharate/Amphetamine Sulf-Aspartate ER, USP, each containing 3.75 mg of Amphetamine Sulfate, 3.75 mg of Amphetamine Aspartate Monohydrate, 3.75 mg of Dextroamphetamine Sulfate, and 3.75 mg of Dextroamphetamine Saccharate. It includes storage instructions, a warning to keep out of reach of children, and dispensing requirements for a child-resistant container. The label also displays the NDC 63629-1974-1, the strength 15 mg, manufacturer, and labeler information.*

* 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.