Atomoxetine Capsule
Product Images NDC 50090-6513

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Atomoxetine (NDC 50090-6513). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by A-s Medication Solutions, 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: Mean Weight And Height Percentiles Over Time For Patients With Three Years Of Atomoxetine Treatment (Atomoxetine Fig1)

Figure 1: Mean Weight And Height Percentiles Over Time For Patients With Three Years Of Atomoxetine Treatment (Atomoxetine Fig1)
Two line graphs depicting mean weight percentile and mean height percentile over months of treatment. The left graph shows mean weight percentile for 203 subjects, displaying a decrease initially and then a gradual increase up to 36 months. The right graph shows mean height percentile for 155 subjects, with relatively stable values over 36 months. Both graphs include error bars.*
FDA Label Image

Chemical Structure (Atomoxetine Str)

Chemical Structure (Atomoxetine Str)
Chemical structure of Atomoxetine hydrochloride, showing its molecular arrangement with aromatic rings and functional groups including an ether linkage and a methylated amine.*
FDA Label Image

Label Image (Lbl500906513)

Label Image (Lbl500906513)
Atomoxetine 40 mg capsules packaging label from A-S Medication Solutions. The label includes the NDC number 50090-6513-0, lot number 6872-0, and states each capsule contains atomoxetine hydrochloride equivalent to 40 mg atomoxetine. Storage instructions specify 68 to 77 degrees Fahrenheit. The package contains 30 capsules.*

* 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.