Dextroamphetamine Sulfate
Product Images NDC 68382-943

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

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Dextroamphetamine Sulfate (NDC 68382-943). 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

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Chemical structure diagram of Dextroamphetamine Sulfate, showing the molecular arrangement including a benzene ring, amine group, and sulfate (H2SO4) component as part of the compound.*
FDA Label Image

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Label for Dextroamphetamine Sulfate Extended-Release Capsules, 5 mg, by Zydus Pharmaceuticals (USA) Inc. The label shows the product brand ZyGenerics, National Drug Code (NDC) 68382-943-01, and states the capsules come in a quantity of 100 with federal law dispensing requirements noted. The product is marked Rx only.*
FDA Label Image

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Dextroamphetamine Sulfate 10 mg Extended-Release Capsules label from Zydus Pharmaceuticals (USA) Inc. It includes the proprietary name, dosage strength, form, and a caution about federal law requiring dispensing with the medication guide. The package contains 100 capsules and is marked Rx only.*
FDA Label Image

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Label of Dextroamphetamine Sulfate Extended-Release Capsules 15 mg from Zydus Pharmaceuticals (USA) Inc. The label includes the NDC number 68382-945-01 and a federal law warning about dispensing with the Medication Guide. The dosage form is extended-release capsules, strength 15 mg.*

* 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.