Dextroamphetamine Sulfate Tablet
Product Images NDC 43386-871

3 FDA label images from Lupin Pharmaceuticals,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 43386-871). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lupin Pharmaceuticals,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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7ef15555-figure-01 (F651f775 5bed 432c A031 Bbb42a2f5387 01)
Chemical structure of dextroamphetamine sulfate showing the molecular arrangement of the active ingredient, including the sulfate group (H2SO4). This structure represents the stereochemistry and functional groups of the drug molecule.*
FDA Label Image

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7ef15555-figure-02 (F651f775 5bed 432c A031 Bbb42a2f5387 02)
Dextroamphetamine Sulfate Tablets USP 5 mg oral tablets label by Lupin Pharmaceuticals, Inc. The label shows a package containing 30 tablets with medication information including dosage strength, storage instructions, and safety warnings. Manufactured by Novel Laboratories, Inc., the label includes a barcode and emphasizes child-resistant packaging and prescription-only status.*
FDA Label Image

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7ef15555-figure-04 (F651f775 5bed 432c A031 Bbb42a2f5387 03)
Dextroamphetamine Sulfate 10 mg tablets packaging label from Lupin Pharmaceuticals, Inc. The label indicates rectangular packaging with orange and blue highlights, specifying 100 tablets. It includes storage instructions, safety warnings, NDC code 43386-871-01, and manufacturing details by Novel Laboratories, Inc. and Lupin Pharmaceuticals, Inc.*

* 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.