Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate And Amphetamine Sulfate Tablet
Product Images NDC 72516-011

6 FDA label images from Oryza Pharmaceuticals Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate And Amphetamine Sulfate (NDC 72516-011). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Oryza 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

Container Label 5 mg (Amphetamines 01 V00)

Container Label 5 mg (Amphetamines 01 V00)
Label of Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets, 5 mg strength, oral tablets manufactured by Oryza Pharmaceuticals Inc. The label shows the NDC number 72516-016-01 and indicates 100 tablets per container. It includes dosage instructions, storage conditions, and a barcode on the right side. The label is primarily white with blue and pink accents.*
FDA Label Image

Container Label 7.5 mg (Amphetamines 02 V00)

Container Label 7.5 mg (Amphetamines 02 V00)
Label of Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets 7.5 mg by Oryza Pharmaceuticals Inc. The label states it contains mixed salts of a single entity amphetamine product, with a quantity of 100 tablets. Storage instructions and dispenser information are included, along with a barcode and NDC 72516-015-01.*
FDA Label Image

Container Label 10 mg (Amphetamines 03 V00)

Container Label 10 mg (Amphetamines 03 V00)
Label for Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets, 10 mg strength, from Oryza Pharmaceuticals Inc. The label shows the product name, strength, dosage form (tablets), quantity (100 tablets), and directions for pharmacists to dispense the medication guide to each patient. It includes storage instructions and manufacturing details.*
FDA Label Image

Container Label 15 mg (Amphetamines 04 V00)

Container Label 15 mg (Amphetamines 04 V00)
Label for Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate 15 mg tablets by Oryza Pharmaceuticals Inc. The label indicates the product contains mixed salts of a single entity amphetamine product, is prescription only, and comes in a bottle of 100 tablets. Storage and dispensing instructions are also provided alongside a barcode.*
FDA Label Image

Container Label 20 mg (Amphetamines 05 V00)

Container Label 20 mg (Amphetamines 05 V00)
Label for Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate tablets, 20 mg strength, supplied by Oryza Pharmaceuticals Inc. The label indicates a package of 100 tablets and includes directions for pharmacist dispensing. Storage instructions and dosage information reference the package insert, with a barcode and NDC number 72516-012-01 present.*
FDA Label Image

Container Label 30 mg (Amphetamines 06 V00)

Container Label 30 mg (Amphetamines 06 V00)
Label for Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate tablets, containing 7.5 mg strength. The bottle contains 100 tablets for oral use. Manufactured by Oryza Pharmaceuticals Inc. The label includes storage instructions, dispensing guidance, and a barcode. It is marked as prescription only (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.