Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate And Amphetamine Sulfate Capsule, Extended Release
Product Images NDC 72162-1379

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 Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate And Amphetamine Sulfate (NDC 72162-1379). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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

Ani.jpg (Ani)

FDA Label Image

Figure-1 (Image 01)

Figure-1 (Image 01)
A pharmacokinetic graph showing mean plasma concentrations of dextroamphetamine and levoamphetamine over 24 hours. It compares extended-release capsules 20 mg once daily and tablets 10 mg twice daily, charting concentration in ng/mL on the y-axis against time in hours on the x-axis.*
FDA Label Image

Label (Lbl721621379)

Label (Lbl721621379)
Label for Mixed Salts of a Single-Entity Amphetamine Product Extended-Release Capsules, 20 mg strength. The label details the composition of each extended-release capsule containing 5 mg each of Amphetamine Sulfate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Dextroamphetamine Saccharate. It is relabeled by Bryant Ranch Prepack and manufactured by ANI Pharmaceuticals, with a package count of 100 capsules. Storage and dispensing instructions are also provided.*

* 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.