Dextroamphetamine Sulfate Tablet
Product Images NDC 27808-090

View Photos of 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 27808-090). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cranbury 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

Barr Structure Formula Pi.jpg (Dextroamphetamine Sulfate Tablets Usp 1)

Barr Structure Formula Pi.jpg (Dextroamphetamine Sulfate Tablets Usp 1)
Chemical structure of Dextroamphetamine Sulfate, showing the molecular arrangement including a benzene ring, amine groups, and sulfate component (H2SO4).*
FDA Label Image

5mg Label (Dextroamphetamine Sulfate Tablets Usp 2)

5mg Label (Dextroamphetamine Sulfate Tablets Usp 2)
Label for Dextroamphetamine Sulfate Tablets USP 5 mg by Cranbury Pharmaceuticals, LLC. The label indicates the product contains 100 tablets with a dosage strength of 5 mg. It includes warnings about the inner seal, storage instructions at 20° to 25°C, a pharmacist dispensing note, and product identification codes with lot, expiration, and serial number placeholders.*
FDA Label Image

10mg Label (Dextroamphetamine Sulfate Tablets Usp 3)

10mg Label (Dextroamphetamine Sulfate Tablets Usp 3)
Dextroamphetamine Sulfate Tablets USP 10 mg oral tablets label from Cranbury Pharmaceuticals, LLC. The label includes warnings about the inner seal, dosage instructions, storage conditions, and keeping the medication out of reach of children. The package contains 100 tablets and is designated Rx 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.