Atomoxetine Capsule
Product Images NDC 70518-4337

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Atomoxetine (NDC 70518-4337). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack 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

Mm2 (Atomoxetine 100mg 70518 4337 01)

Mm2 (Atomoxetine 100mg 70518 4337 01)
Label for Atomoxetine 100 mg capsule repackaged by RemedyRepack Inc. It includes dosage strength, quantity of 1 capsule, storage instructions, and original manufacturer Dr. Reddy's in Shreveport, LA. Also features NDC numbers and a QR code, with a reminder that the product is RX only.*
FDA Label Image

Remedy_label (Remedy Label)

Remedy_label (Remedy Label)
Atomoxetine 100 mg capsule label for oral use by RemedyRepack Inc. Contains 30 capsules per box. Label displays NDC 70518-4337-00 and repackager contact information from Indiana, PA. Includes storage instructions and original manufacturer as Dr. Reddy's, Shreveport, LA.*
FDA Label Image

Graph (Graph)

Graph (Graph)
Two line graphs showing mean weight percentile and mean height percentile over 36 months of treatment. The left graph with N=203 indicates mean weight percentile trends, and the right graph with N=155 displays mean height percentile trends, both with error bars representing variation.*
FDA Label Image

Structure (Structure)

Structure (Structure)
Chemical structure of atomoxetine hydrochloride, showing its molecular framework including aromatic rings, methyl group, and hydrochloride salt component.*

* 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.