Dextroamphetamine Sulfate
Product Images NDC 68382-941

3 FDA label images from Zydus Pharmaceuticals (usa) Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Dextroamphetamine Sulfate (NDC 68382-941). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zydus Pharmaceuticals (usa) 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

Chemical Structure (Ad840fb3 5860 447a 8ad3 61c29d883733 01)

Chemical Structure (Ad840fb3 5860 447a 8ad3 61c29d883733 01)
Chemical structure of dextroamphetamine sulfate showing two molecules of the dextroamphetamine cation paired with one sulfate anion (H2SO4). The structure includes a benzene ring attached to a chiral carbon with an amine group.*
FDA Label Image

5 mg Bottle Label (Ad840fb3 5860 447a 8ad3 61c29d883733 02)

5 mg Bottle Label (Ad840fb3 5860 447a 8ad3 61c29d883733 02)
Dextroamphetamine Sulfate Tablets, USP 5 mg label from Zydus Pharmaceuticals (USA) Inc. The label includes the brand ZyGenerics, NDC 68382-941-01, and states 'Rx only' with a package size of 100 tablets. It instructs the pharmacist to dispense the accompanying medication guide.*
FDA Label Image

10 mg Bottle Label (Ad840fb3 5860 447a 8ad3 61c29d883733 03)

10 mg Bottle Label (Ad840fb3 5860 447a 8ad3 61c29d883733 03)
Label for Dextroamphetamine Sulfate Tablets, USP 10 mg by Zydus Pharmaceuticals (USA) Inc. The label includes the NDC number 68382-942-01, instructions for pharmacists to dispense the medication guide, and states the product contains 10 tablets for prescription use only.*

* 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.