Dextroamphetamine Sulfate
Product Images NDC 58177-312

3 FDA label images from Ethex Corporation · 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 58177-312). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ethex Corporation, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Structural Formula (Dextroamphe Sl Tb 01)

Structural Formula (Dextroamphe Sl Tb 01)
Chemical structure diagram of dextroamphetamine sulfate, showing the molecular arrangement of the active ingredient associated with the Ethex Corporation product.*
FDA Label Image

5 mg Bottle Label (Dextroamphe Sl Tb 02)

5 mg Bottle Label (Dextroamphe Sl Tb 02)
Dextroamphetamine Sulfate Tablets USP 5 mg label from Ethex Corporation. The label indicates each tablet contains 5 mg dextroamphetamine sulfate, with a bottle count of 100 tablets. It includes storage instructions (20°-25°C), a warning to keep out of children’s reach, and mentions dosage and dispensing guidelines. The label displays the NDC 58177-311-04 and manufacturer information for KV Pharmaceutical Co. for Ethex Corporation in St. Louis, MO.*
FDA Label Image

10 mg Bottle Label (Dextroamphe Sl Tb 03)

10 mg Bottle Label (Dextroamphe Sl Tb 03)
Dextroamphetamine Sulfate Tablets, USP 10 mg by Ethex Corporation in a 100-tablet package. The label includes the NDC 58177-312-04, dosage instructions, storage conditions, and warnings to keep out of reach of children and to dispense medication guide with each prescription.*

* 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.