Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate And Amphetamine Sulfate Capsule, Extended Release
Product Images NDC 70010-030

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 70010-030). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Granules Pharmaceuticals 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

10-mg-container-label (10 mg)

Label for extended-release capsules containing Mixed Salts of a Single Entity Amphetamine Product with 10 mg strength. The label lists active ingredients including dextroamphetamine saccharate, amphetamine aspartate monohydrate, dextroamphetamine sulfate, and amphetamine sulfate. It states 100 capsules in the package, prescription only, and is manufactured by Granules Pharmaceuticals Inc., Chantilly, VA. Contains storage instructions and barcode.*

FDA Label Image

15-mg-container-label (15 mg)

Label for extended-release capsules containing dextroamphetamine saccharate, amphetamine aspartate monohydrate, dextroamphetamine sulfate, and amphetamine sulfate with a strength of 15 mg. The label includes storage instructions, a barcode, and states the product is manufactured by Granules Pharmaceuticals Inc. The package contains 100 capsules and is Rx only.*

FDA Label Image

20-mg-container-label (20 mg)

Label for 20 mg extended-release capsules of mixed salts of a single entity amphetamine product containing dextroamphetamine saccharate, amphetamine aspartate monohydrate, dextroamphetamine sulfate, and amphetamine sulfate. The label indicates 100 capsules per container, is for prescription use only, and is manufactured by Granules Pharmaceuticals Inc. Storage and handling instructions, along with a barcode and NDC 70010-032-01, are also displayed.*

FDA Label Image

25-mg-container-label (25 mg)

Label for dextroamphetamine saccharate, amphetamine aspartate monohydrate, dextroamphetamine sulfate, and amphetamine sulfate extended-release capsules, 25 mg strength. The label shows 100 capsules per container, marked Rx only, manufactured by Granules Pharmaceuticals Inc. It includes storage instructions, a barcode, and reference to the medication guide and package insert for complete information.*

FDA Label Image

30-mg-container-label (30 mg)

Label for Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate extended-release capsules, 30 mg strength. The label indicates it is a mixed salts single entity amphetamine product, contains 100 capsules, and is for Rx only. It is manufactured by Granules Pharmaceuticals Inc., Chantilly, VA. The label includes storage instructions, barcode, and a note to dispense the medication guide.*

FDA Label Image

5-mg-container-label (5 mg)

Label for dextroamphetamine saccharate, amphetamine aspartate monohydrate, dextroamphetamine sulfate and amphetamine sulfate extended-release capsules 5 mg. The label includes dosage details, storage instructions, manufacturer information for Granules Pharmaceuticals Inc., and packaging quantity of 100 capsules. It features a barcode and advises dispensing the medication guide separately to patients.*

FDA Label Image

Figure-1 (Figure 1)

A line graph comparing mean plasma concentrations of dextroamphetamine and levoamphetamine over 24 hours for extended-release capsules and tablets. The x-axis represents time in hours, and the y-axis represents mean plasma concentrations in ng/mL. Four lines show concentration profiles for capsules and tablets of both isomers at different dosages.*

* 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.