Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate And Amphetamine Sulfate Tablet
Product Images NDC 0527-0761

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate And Amphetamine Sulfate (NDC 0527-0761). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lannett Company, 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

Label (Dex Sac Amp Asp Dex Sul And Amp Sul 1)

Packaging label for Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets, 5 mg strength. The label shows dosage details, a barcode, 100 tablet count, and is distributed by Lannett Company, LLC. It includes storage and medication guide instructions and a warning to keep medication out of reach of children.*

FDA Label Image

Label (Dex Sac Amp Asp Dex Sul And Amp Sul 2)

Label for Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets, 7.5 mg strength, in a tablet dosage form. The label states the product contains mixed salts of a single-entity amphetamine product and is distributed by Lannett Company, LLC. The package contains 100 tablets, with directions to keep medication out of reach of children and to see prescription information for dosage. It includes a barcode and emphasizes dispensing the Medication Guide to patients.*

FDA Label Image

Label (Dex Sac Amp Asp Dex Sul And Amp Sul 3)

Label for Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate 10 mg tablets. The label states the active ingredients and strength with a note that tablets contain 2.5 mg of each amphetamine component per unit. It includes storage instructions, dosage guidance references, and a warning to keep medication out of children’s reach. The product is distributed by Lannett Company, LLC, with a package count of 100 tablets and barcode visible.*

FDA Label Image

Label (Dex Sac Amp Asp Dex Sul And Amp Sul 4)

Label for Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets 12.5 mg by Lannett Company, LLC. The label shows the active ingredient strengths, dosage form as tablets, prescription use only, package size of 100 tablets, storage instructions, and a barcode.*

FDA Label Image

Label (Dex Sac Amp Asp Dex Sul And Amp Sul 5)

Label for Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets, 15 mg strength, oral tablet form, supplied by Lannett Company, LLC. The label includes a drug description, NDC 0527-0764-37, dosage instructions, storage conditions, and a 100-count package size. The product is identified as prescription only (Rx Only).*

FDA Label Image

Label (Dex Sac Amp Asp Dex Sul And Amp Sul 6)

Label for Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets 20 mg by Lannett Company, LLC. The label includes active ingredient amounts per tablet, storage instructions, dispensing guidance, quantity of 100 tablets, and a barcode.*

FDA Label Image

Label (Dex Sac Amp Asp Dex Sul And Amp Sul 7)

Label for Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets 30 mg, containing mixed salts of a single-entity amphetamine product. The label indicates a count of 100 oral tablets, distributed by Lannett Company, LLC. It includes storage instructions, dosage warnings, and a medication guide reference.*

* 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.