Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, And Amphetamine Sulfate Capsule, Extended Release
Product Images NDC 66993-599

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 66993-599). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Prasco Laboratories, 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 1 (Adderall 01)

Line graph showing mean plasma concentrations of dextroamphetamine and levoamphetamine over 24 hours following administration of MAS-ER 20 mg once daily and Adderall 10 mg twice daily. The graph distinguishes between dextroamphetamine and levoamphetamine levels, with time in hours on the x-axis and mean plasma concentration (ng/mL) on the y-axis.*

FDA Label Image

Principal Display Panel (5 mg Capsule Bottle Label)

Label for Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate extended-release capsules 5 mg by Prasco Laboratories. The label states the product is a mixed salt amphetamine extended-release capsule, available in a 100-capsule supply, for prescription use only. Storage instructions and a barcode are also visible.*

FDA Label Image

Principal Display Panel (10 mg Capsule Bottle Label)

Label for Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate extended-release capsules, 10 mg strength. The label indicates 100 capsules per bottle, distributed by Prasco Laboratories. It includes storage instructions and active ingredient amounts per capsule and states the product is prescription only (Rx only).*

FDA Label Image

Principal Display Panel (15 mg Capsule Bottle Label)

Label for Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate extended-release capsules, 15 mg strength. The label shows it contains 100 capsules and is distributed by Prasco Laboratories. Storage instructions and dosage details are also included in the label.*

FDA Label Image

Principal Display Panel (20 mg Capsule Bottle Label)

Label for Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate extended-release capsules, 20 mg, distributed by Prasco Laboratories. The label indicates a package size of 100 capsules, prescription only, with instructions to dispense with an attached medication guide. Storage and handling instructions are also noted.*

FDA Label Image

Principal Display Panel (25 mg Capsule Bottle Label)

Label for Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate extended-release capsules, 25 mg strength. The label indicates the product contains 100 capsules and is prescription only. It is distributed by Prasco Laboratories, Mason, OH, and includes storage and dispensing instructions. The design features the Prasco logo and a green wave graphic.*

FDA Label Image

Principal Display Panel (30 mg Capsule Bottle Label)

Label for Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate extended-release capsules, 30 mg strength. The label shows that the product contains 100 capsules, is prescription only, and is distributed by Prasco Laboratories. It includes storage instructions, a barcode, and product information indicating it is a mixed salts amphetamine product.*

* 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.