Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, And Amphetamine Sulfate Tablet
Product Images NDC 57664-643

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 57664-643). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, 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

Principal Display Panel (5 mg Tablet Bottle Label)

Label for Dextroamphetamine saccharate, amphetamine aspartate, dextroamphetamine sulfate, and amphetamine sulfate tablets containing 5 mg strength. The label includes the NDC number 57664-641-08, indicates it is a prescription drug with 100 tablets per container, and is distributed by Sun Pharmaceutical Industries, Inc. Additional dosage and dispensing information for pharmacists is also present.*

FDA Label Image

Principal Display Panel (7.5 mg Tablet Bottle Label)

Label for Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets 7.5 mg by Sun Pharmaceutical Industries, Inc. The label states the product is prescription only, contains 100 tablets, and includes a pharmacist warning to dispense with medication guide. The active ingredients' strengths sum to 7.5 mg total. Storage and dosing instructions are noted in small print on the label.*

FDA Label Image

Principal Display Panel (10 mg Tablet Bottle Label)

Label for Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets, 10 mg strength. The oral tablet is distributed by Sun Pharmaceutical Industries, Inc., and supplied in a container of 100 tablets. The label includes a dosage guide warning for pharmacists and storage instructions, along with a barcode and regulatory information.*

FDA Label Image

Principal Display Panel (12.5 mg Tablet Bottle Label)

Label for Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets, 12.5 mg strength. The label shows a package containing 100 tablets, for oral use. It includes dispensing instructions and branding by Sun Pharmaceutical Industries, Inc. The label features dosage details and storage instructions.*

FDA Label Image

Principal Display Panel (15 mg Tablet Bottle Label)

Label for Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets 15 mg by Sun Pharmaceutical Industries, Inc. The oral tablets come in a 100-count bottle, indicated as Rx only. The label includes dosing information, storage instructions, and a barcode.*

FDA Label Image

Principal Display Panel (20 mg Tablet Bottle Label)

Label for Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets 20 mg by Sun Pharmaceutical Industries, Inc. The label states a package of 100 tablets, prescription only, and includes dispensing instructions and storage information. It also shows a barcode and NDC 57664-646-08.*

FDA Label Image

Principal Display Panel (30 mg Tablet Bottle Label)

Label for Dextroamphetamine saccharate, Amphetamine aspartate, Dextroamphetamine sulfate, and Amphetamine sulfate Tablets 30 mg by Sun Pharmaceutical Industries, Inc. The label indicates a mixed salts amphetamine product containing 100 tablets for oral use, with a prescription-only designation. It includes dispensing instructions, dosage warnings, and storage information.*

* 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.