Atomoxetine Capsule
Product Images NDC 71335-3033

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 71335-3033). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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

Image (27a196c2 92d8 4c4f 97e5 210ae78dedbe 01)

Image (27a196c2 92d8 4c4f 97e5 210ae78dedbe 01)
Two line graphs showing the mean weight percentile and mean height percentile over 36 months of treatment. The left graph tracks mean weight percentile for 203 subjects, demonstrating a decline followed by stabilization and a gradual increase. The right graph tracks mean height percentile for 155 subjects, showing a slight decline that stabilizes over time.*
FDA Label Image

Image (27a196c2 92d8 4c4f 97e5 210ae78dedbe 02)

Image (27a196c2 92d8 4c4f 97e5 210ae78dedbe 02)
Chemical structure diagram of atomoxetine hydrochloride, showing the molecular arrangement including aromatic rings, methyl group, oxygen atom, and hydrochloride component, consistent with the active ingredient atomoxetine.*
FDA Label Image

Label (Lbl713353033)

Label (Lbl713353033)
Label for Atomoxetine Capsules USP, 40 mg strength, manufactured by Strides Pharma Science Limited and relabeled by Bryant Ranch Prepack. The label indicates a package size of 30 oral capsules, includes the NDC 71335-3033-1, and storage instructions between 20°C to 25°C with permitted excursions. It advises dispensing with a medication guide and storing in a child-resistant container.*

* 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.