Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, Amphetamine Sulfate Extended-release
Product Images NDC 57664-341

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, Amphetamine Sulfate Extended-release (NDC 57664-341). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, 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 (Amphetamines 01)

A line graph depicting mean plasma concentrations of dextroamphetamine and levoamphetamine over 24 hours. The x-axis shows time in hours, and the y-axis indicates mean plasma concentrations. Two types of dosage forms are compared: extended-release capsules of 20 mg taken once daily and tablets of 10 mg taken twice daily. Lines differentiate between dextroamphetamine and levoamphetamine levels for each dosage regimen.*

FDA Label Image

Pdp-5mg (Amphetamines 02)

Label for Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, Amphetamine Sulfate Extended-Release Capsules 5 mg by Sun Pharmaceutical Industries, Inc. The label states that each capsule contains mixed salts of a single entity amphetamine product with 5 mg strength and includes 100 capsules per bottle. It provides storage instructions, pharmacist dispensing guidance, and includes barcodes and NDC number 57664-336-88.*

FDA Label Image

Pdp-10mg (Amphetamines 03)

Label for Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, Amphetamine Sulfate Extended-Release Capsules 10 mg by Sun Pharmaceutical Industries, Inc. The label lists dosing information, NDC 57664-337-88, and warnings including pharmacist dispensing instructions and storage conditions. The package size is 100 capsules.*

FDA Label Image

Pdp-15mg (Amphetamines 04)

Label for Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, Amphetamine Sulfate Extended-Release Capsules 15 mg by Sun Pharmaceutical Industries, Inc. The label states 100 capsules, Rx only, with detailed active ingredient amounts per capsule and storage instructions. It includes manufacturer and distributor information, barcodes, and a serialization instruction area.*

FDA Label Image

Pdp-20mg (Amphetamines 05)

Label for Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, Amphetamine Sulfate Extended-Release Capsules 20 mg. The label shows the active ingredients and strengths per capsule, directs pharmacists to dispense with a medication guide, and indicates the package contains 100 capsules. Manufactured by Sun Pharmaceutical Industries, Inc., with storage and safety information. Barcodes and NDC 57664-339-88 are included on the label.*

FDA Label Image

Pdp-25m (Amphetamines 06)

Label for Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, Amphetamine Sulfate Extended-Release Capsules 25 mg by Sun Pharmaceutical Industries, Inc. The label includes the NDC number 57664-340-88 and information on capsule strength, quantity (100 capsules), and handling instructions including Rx Only and pharmacist dispensing guidance.*

FDA Label Image

Pdp-30mg (Amphetamines 07)

Label for Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, Amphetamine Sulfate Extended-Release Capsules 30 mg from Sun Pharmaceutical Industries, Inc. The label includes active ingredient strengths, pharmacy dispensing instructions, quantity (100 capsules), storage conditions, 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.