Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, And Amphetamine Sulfate Tablet
Product Images NDC 42858-727

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, And Amphetamine Sulfate (NDC 42858-727). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rhodes Pharmaceuticals Llc, 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, 5 mg strength. The label indicates the product is prescription only, with a package size of 100 tablets. It includes storage instructions, a pharmacist dispensing note about the medication guide, and is labeled by Rhodes Pharmaceuticals LLC.*

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 Rhodes Pharmaceuticals LLC. The label notes it is a mixed salts single-entity amphetamine product for oral use. The package contains 100 tablets and notes pharmacist dispensing instructions and storage conditions. Includes an NDC barcode and safety warnings.*

FDA Label Image

Principal Display Panel (10 mg Tablet Bottle Label)

Label for Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets, containing 10 mg strength. The label specifies it as a mixed salts of a single-entity amphetamine product, with a quantity of 100 tablets. It includes storage instructions, pharmacist dispensing guidance, and a barcode. Labeler is Rhodes Pharmaceuticals LLC.*

FDA Label Image

Principal Display Panel (12.5 mg Tablet Bottle Label)

Label for Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets 12.5 mg. The label indicates the product is prescription-only, comes in a package of 100 tablets, and is manufactured by Rhodes Pharmaceuticals LLC. Storage instructions and a barcode are also visible.*

FDA Label Image

Principal Display Panel (15 mg Tablet Bottle Label)

Label for Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets containing 15 mg strength. The label indicates a prescription drug by Rhodes Pharmaceuticals LLC, with a package size of 100 tablets. Storage instructions and a reminder to dispense the accompanying medication guide are also included.*

FDA Label Image

Principal Display Panel (20 mg Tablet Bottle Label)

Label of Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets, 20 mg. The label includes dosing instructions, pharmacy dispensing guidance, storage conditions, and the product is presented in a 100-tablet package by Rhodes Pharmaceuticals LLC. The label also features a barcode and an NDC number 42858-726-01.*

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 strength. The label indicates this is a prescription-only medication supplied by Rhodes Pharmaceuticals LLC and contains 100 tablets. Storage instructions and a caution to dispense the accompanying medication guide are also shown.*

* 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.