Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, And Amphetamine Sulfate Capsule, Extended Release
Product Images NDC 0781-2352

7 FDA label images from Sandoz Inc · Packaging, Regulatory Labels, and Product Appearance

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 0781-2352). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sandoz 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 1 (Dextroamphetamine 01)

Figure 1 (Dextroamphetamine 01)
A line graph comparing mean plasma concentrations (ng/mL) of dextroamphetamine and levoamphetamine over 24 hours. It plots time (hours) on the x-axis versus plasma concentration on the y-axis. Four lines represent MAS-ER 20 mg once daily and Adderall 10 mg twice daily for both dextroamphetamine and levoamphetamine.*
FDA Label Image

Principal Display Panel (5 mg Capsule Bottle Label)

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 strength. The label indicates 100 capsules per bottle, distributed by Sandoz Inc. It includes storage instructions and a barcode.*
FDA Label Image

Principal Display Panel (10 mg Capsule Bottle Label)

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 states it is a mixed salts of a single-entity amphetamine product, Rx only, containing 100 capsules. Distributed by Sandoz Inc, Princeton, NJ. The label includes storage instructions and dosage details.*
FDA Label Image

Principal Display Panel (15 mg Capsule Bottle Label)

Principal Display Panel (15 mg Capsule Bottle Label)
Label for extended-release capsules containing Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate, 15 mg strength. The label notes it is a mixed salts single-entity amphetamine product, prescription only, with 100 capsules per container. Distributed by Sandoz Inc, Princeton, NJ. Includes storage instructions and a barcode.*
FDA Label Image

Principal Display Panel (20 mg Capsule Bottle Label)

Principal Display Panel (20 mg Capsule Bottle Label)
Label for Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate extended-release capsules by Sandoz. The label indicates a 20 mg strength, contains 100 capsules, and notes the product is Rx only. It includes storage instructions, barcodes, and mentions the medication guide for pharmacists to dispense to patients.*
FDA Label Image

Principal Display Panel (25 mg Capsule Bottle Label)

Principal Display Panel (25 mg Capsule Bottle Label)
Packaging label for Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate extended-release capsules, 25 mg strength. The label shows 'Rx Only' status, quantity of 100 capsules, and is distributed by Sandoz Inc. It includes storage instructions and mentions the product as mixed salts of a single-entity amphetamine product.*
FDA Label Image

Principal Display Panel (30 mg Capsule Bottle Label)

Principal Display Panel (30 mg Capsule Bottle Label)
Label for Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate extended-release capsules. The label indicates 30 mg strength and a bottle containing 100 capsules. Distributed by Sandoz Inc, the label includes storage instructions, a barcode, and a note stating the medication guide must be dispensed to patients.*

* 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.