Amphetamine Sulfate Tablet
Product Images NDC 52536-057

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Amphetamine Sulfate (NDC 52536-057). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Wilshire 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

Chemical Structure (Amphetamine 01)

Chemical structure of amphetamine sulfate showing the amphetamine cation with an attached ammonium group and the sulfate anion in the formula.*

FDA Label Image

Principal Display Panel (5 mg Tablet Bottle Label)

Amphetamine Sulfate Tablets USP 5 mg oral tablets packaging label by Wilshire Pharmaceuticals, Inc. The label includes dosage strength, NDC number 52536-057-10, quantity of 100 tablets, prescription only status, storage conditions, and a pharmacist dispensing instruction to provide the Medication Guide separately.*

FDA Label Image

Amphetamine 02a

Amphetamine Sulfate Tablets USP, 5 mg strength, oral tablet form, packaged with 30 tablets, labeled for prescription use only. The label includes storage instructions, a warning to keep out of reach of children, and tamper-evident information. Manufactured for Wilshire Pharmaceuticals, Inc., Atlanta, GA.*

FDA Label Image

Principal Display Panel (10 mg Tablet Bottle Label)

Label for Amphetamine Sulfate Tablets, USP 10 mg oral tablets by Wilshire Pharmaceuticals, Inc. The label includes NDC 52536-059-10, states prescription use only, and provides storage instructions at 20° to 25° C with tamper-evident foil seal under the cap. It advises dispensing in a well-closed container and keeping out of reach of children.*

FDA Label Image

Amphetamine 04

Amphetamine Sulfate Tablets, USP 10 mg oral tablets label from Wilshire Pharmaceuticals, Inc. The label includes product strength, dosage form, NDC number 52536-059-03, prescription-only status, storage instructions, and a warning to keep out of reach of children. The package contains 30 tablets.*

* 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.