Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate And Amphetamine Sulfate Capsule, Extended Release
Product Images NDC 43975-277

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate And Amphetamine Sulfate (NDC 43975-277). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ani 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

Figure-1 (Image 01)

A line graph depicting mean plasma concentrations of dextroamphetamine and levoamphetamine over 24 hours after administration of extended-release capsules and tablets containing a combination of dextroamphetamine saccharate, amphetamine aspartate, dextroamphetamine sulfate, and amphetamine sulfate. The x-axis represents time in hours, and the y-axis shows mean plasma concentration in ng/mL, comparing different dosage forms and dosing schedules.*

FDA Label Image

Anilogo (Ani Small)

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Anilogo (Ani Small 01)

FDA Label Image

Label-5mg (Label 5mg)

Label for Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate extended-release capsules, 5 mg strength. The label shows it is a mixed salts single-entity amphetamine product with 100 capsules per bottle, distributed by ANI Pharmaceuticals, Inc. The label includes active ingredient amounts per capsule, storage instructions, and a barcode with serial and lot numbers.*

FDA Label Image

Label-10mg (Label 10mg)

Label for Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate extended-release capsules 10 mg. The label includes active ingredient strengths of 2.5 mg each per extended-release capsule, dosing and storage instructions, a barcode, serialization data, and is distributed by ANI Pharmaceuticals, Inc. The package contains 100 capsules and is designated as a Schedule II controlled substance.*

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Label-15mg (Label 15mg)

Label for Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate extended-release capsules, 15 mg strength. The label indicates it contains 100 capsules, is distributed by ANI Pharmaceuticals, Inc., Baudette, MN, and includes dosage and storage instructions along with a barcode and serial, lot, and expiry placeholders.*

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Label-20mg (Label 20mg)

Label for Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate 20 mg extended-release capsules. The label includes the drug's mixed amphetamine salts composition, package size of 100 capsules, and distribution by ANI Pharmaceuticals, Inc. It features dosage and storage instructions, a barcode, and a QR code with serial number, lot, and expiration placeholders.*

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Label-25mg (Label 25mg)

Label for Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate extended-release capsules, 25 mg strength. The label indicates a package size of 100 capsules, distributed by ANI Pharmaceuticals, Inc. The label includes dosage composition details, storage instructions, a barcode, and a serial number section.*

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Label-30mg (Label 30mg)

Label for Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate Extended-Release Capsules CII 30 mg. The label states the drug as mixed salts of a single-entity amphetamine product, with a package size of 100 capsules. Distributed by ANI Pharmaceuticals, Inc., Baudette, MN. Includes dosage strength, storage instructions, a barcode, and serialization details.*

* 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.