Atomoxetine Hydrochloride Capsule
Product Images NDC 50268-058

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Atomoxetine Hydrochloride (NDC 50268-058). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Avpak, 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

25mg (057 13 25mg)

Label for Atomoxetine Capsules, USP 25 mg by AvPAK, a human prescription drug in oral capsule form. The label shows the NDC 50268-057-13 and indicates a package size of 30 capsules (3 x 10 unit dose). It includes storage instructions, dispensing advice, and manufacturer information for AvKARE, Pulaski, TN. The AvPAK logo is visible at the bottom.*

FDA Label Image

40mg (058 13 40mg)

Packaging label for Atomoxetine Capsules, USP, 40 mg oral capsules. The label indicates prescription only with a package size of 30 capsules (3 blister cards of 10). Manufactured by AvPAK for AvKARE, Pulaski, TN. Storage and dispensing instructions, including guidance for pharmacists, are included on the label.*

FDA Label Image

Atomfig1 (Atomfig1)

Two line graphs showing mean weight and height percentiles over 36 months of treatment. The left graph depicts mean weight percentile changes in a sample of 203 subjects, while the right graph shows mean height percentile changes in 155 subjects during the same period.*

FDA Label Image

Atomstructure (Atomstructure)

Chemical structure diagram of atomoxetine hydrochloride, the active ingredient in Atomoxetine Hydrochloride 25 mg and 40 mg capsules. The diagram shows the molecular arrangement including aromatic rings and functional groups, accompanied by the hydrochloride (HCl) 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.