Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate And Amphetamine Sulfate Tablet
Product Images NDC 11534-196

14 FDA label images from Sunrise Pharmaceutical, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 14 technical images submitted to the FDA as part of the official labeling for Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate And Amphetamine Sulfate (NDC 11534-196). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sunrise Pharmaceutical, 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.

Product Images & Figures Index

FDA Label Image

Figure-5mg-100 (Label 5 100)

Figure-5mg-100 (Label 5 100)
Label for Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets, 5 mg strength. The label specifies these tablets as mixed salts of a single entity amphetamine product with a package size of 100 tablets. The labeler is Sunrise Pharmaceutical, Inc. Additional dispensing instructions and storage conditions are also visible.*
FDA Label Image

Figure-5mg-1000 (Figure 5mg 1000)

Figure-5mg-1000 (Figure 5mg 1000)
Label for Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, and Amphetamine Sulfate 5 mg tablets. The label indicates the product contains 1000 tablets, is prescription only, and packaged by Sunrise Pharmaceutical, Inc. It includes dosing, storage instructions, and a barcode.*
FDA Label Image

Figure-75mg-100 (Label 75 100)

Figure-75mg-100 (Label 75 100)
Label for Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets, 7.5 mg strength, distributed by Sunrise Pharma. The label indicates it contains 100 tablets and is for prescription use only (Rx only). It includes the NDC number 11534-191-01 and specifies that a Medication Guide should be dispensed to each patient.*
FDA Label Image

Figure-75mg-1000 (Figure 75mg 1000)

Figure-75mg-1000 (Figure 75mg 1000)
Label for Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets, a mixed salts amphetamine product, 7.5 mg strength. The label includes the NDC number 11534-191-03, states 'Rx only,' and indicates the package contains 1000 tablets. It includes usage instructions, storage conditions, and warnings, with the labeler identified as Sunrise Pharmaceutical, Inc.*
FDA Label Image

Figure-10mg-100 (Label 10 100)

Figure-10mg-100 (Label 10 100)
Label for Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate tablets, 10 mg strength, by Sunrise Pharmaceutical, Inc. The label includes the NDC number 11534-192-01, indicates Rx only, contains 100 tablets, and directions for the pharmacist to dispense the Medication Guide separately to each patient.*
FDA Label Image

Figure-10mg-1000 (Figure 10mg 1000)

Figure-10mg-1000 (Figure 10mg 1000)
Label for Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, and Amphetamine Sulfate 10 mg tablets by Sunrise Pharmaceutical, Inc. The label shows the active ingredient strengths per tablet as mixed salts of amphetamine, packaging of 1000 tablets, and a note that the package is not child-resistant. It includes usage directions, storage conditions, and a barcode.*
FDA Label Image

Figure-125mg-100 (Label 125 100)

Figure-125mg-100 (Label 125 100)
Label for Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets 12.5 mg by Sunrise Pharmaceutical, Inc. The label includes the active ingredients, strength 12.5 mg, quantity of 100 tablets, and a note to dispense the Medication Guide separately to each patient. It features a barcode and NDC 11534-193-01.*
FDA Label Image

Figure-125mg-1000 (Figure 125mg 1000)

Figure-125mg-1000 (Figure 125mg 1000)
Label for Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets 12.5 mg by Sunrise Pharma. The label states it contains 1000 tablets and is not child-resistant. It includes dosage information, storage instructions, and dispensing guidance for pharmacists, along with barcode and regulatory details.*
FDA Label Image

Image Description (Label 15 100)

Image Description (Label 15 100)
Label for Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets 15 mg by Sunrise Pharmaceutical, Inc. The label states this product contains mixed salts of a single entity amphetamine and includes 100 tablets. It also includes dispensing instructions for pharmacists and a National Drug Code (NDC) number 11534-194-01.*
FDA Label Image

Figure-15mg-1000 (Figure 15mg 1000)

Figure-15mg-1000 (Figure 15mg 1000)
Label for Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets, 15 mg strength. The label shows the product name with active ingredients listed as mixed salts of a single entity amphetamine product. It states the package contains 1000 tablets, is not child-resistant, and is manufactured and distributed by Sunrise Pharmaceutical, Inc. The label includes dosage information, storage instructions, and a barcode.*
FDA Label Image

Figure-20mg-100 (Label 20 100)

Figure-20mg-100 (Label 20 100)
Label for Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets 20 mg by Sunrise Pharmaceutical, Inc. The label displays the product name, strength, and the count of 100 tablets. It includes dosing information and cautionary statements. The strip code and NDC number 11534-195-01 are visible.*
FDA Label Image

Figure-20mg-1000 (Figure 20mg 1000)

Figure-20mg-1000 (Figure 20mg 1000)
Label for Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets 20 mg by Sunrise Pharma. The label indicates these are mixed salts of a single entity amphetaminic product, with a package size of 1000 tablets. It includes dispensing instructions, storage conditions, and warnings that the package is not child-resistant.*
FDA Label Image

Figure-30mg-100 (Label 30 100)

Figure-30mg-100 (Label 30 100)
Label for Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets, 30 mg strength. The label indicates it is a prescription medication with 100 tablets per container, distributed by Sunrise Pharma. It includes the National Drug Code (NDC) 11534-196-01, barcode, dosing information, and standardized warnings.*
FDA Label Image

Figure-30mg-1000 (Figure 30mg 1000)

Figure-30mg-1000 (Figure 30mg 1000)
Label for Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, and Amphetamine Sulfate tablets, 30 mg strength. The label indicates the product contains mixed salts of a single entity and is supplied by SUNRISE PHARMACEUTICAL, INC. It includes dispensing instructions, a warning that the package is not child-resistant, and the quantity of 1000 tablets. Additional information includes usage directions, handling precautions, and a barcode.*

* 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.