Strattera Capsule
Product Images NDC 0002-3228

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Strattera (NDC 0002-3228). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Eli Lilly And Company, 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 (Strattera2)

Two line charts showing changes over 36 months in mean weight percentile and mean height percentile for a group of patients, with sample sizes of 203 and 155 respectively. The x-axes represent months of treatment, and the y-axes represent mean percentile values for weight and height, including error bars indicating variability.*

FDA Label Image

Chemical Structure (Strattera1)

Chemical structure of Atomoxetine hydrochloride, the active ingredient in Strattera capsules, showing the molecular arrangement including aromatic rings and functional groups.*

FDA Label Image

Package Label (STRATTERA 10 mg bottle of 30)

Strattera 10 mg atomoxetine capsules package label displaying 30 capsules. The label includes the NDC 0002-3227-30, Eli Lilly and Company as the labeler, and highlights the dosage strength of 10 mg. It features usage warnings about the Lilly inner seal and storage instructions, along with a barcode and directions to keep out of reach of children.*

FDA Label Image

Package Label (STRATTERA 18 mg bottle of 30)

Packaging label for Strattera 18 mg capsules by Eli Lilly and Company. The label indicates 30 capsules per container, with each capsule equivalent to 18 mg atomoxetine. The label shows the prescription-only status, a barcode, NDC 0002-3238-30, and storage instructions at 25°C with temperature excursions allowed. It includes a warning about the Lilly inner seal and directs to www.strattera.com for more information.*

FDA Label Image

Package Label (STRATTERA 25 mg bottle of 30)

Label for Strattera 25 mg capsules by Eli Lilly and Company. It indicates the product contains 30 capsules of atomoxetine capsules for oral use. The label features the NDC 0002-3228-30, prescription only status, and a warning not to use if the Lilly inner seal is missing or broken. Storage and marketing information is also present.*

FDA Label Image

Package Label (STRATTERA 40 mg bottle of 30)

Label for Strattera 40 mg capsules, containing atomoxetine hydrochloride. The label shows a blue and white capsule image, indicating each capsule is equivalent to 40 mg atomoxetine. The product is prescription-only and marketed by Eli Lilly and Company. The label includes storage instructions, a barcode, NDC 0002-3229-30, and the website www.strattera.com.*

FDA Label Image

Package Label (STRATTERA 60 mg bottle of 30)

Strattera 60 mg capsules label by Eli Lilly and Company. The label shows a blue and yellow capsule image, states the strength as 60 mg atomoxetine, and includes 30 capsules per package. It features storage instructions, barcode, NDC 0002-3239-30, and branding with the Strattera name and Lilly logo.*

FDA Label Image

Package Label (STRATTERA 80 mg bottle of 30)

Strattera 80 mg capsules label by Eli Lilly and Company, indicating 30 capsules per package. The label shows the proprietary name Strattera and the generic name atomoxetine capsules. It includes dosing information stating each capsule is equivalent to 80 mg atomoxetine, and warnings about the Lilly inner seal. The label also displays storage instructions, NDC 0002-3250-30, barcode, and manufacturer details.*

FDA Label Image

Package Label (STRATTERA 100 mg bottle of 30)

Strattera 100 mg atomoxetine capsules label shows 30 capsules with prescription-only designation. The label features an image of a capsule, states each capsule is equivalent to 100 mg atomoxetine, and includes warnings about the integrity of the Lilly inner seal. Manufactured by Eli Lilly and Company, the label also provides storage instructions, a website, lot and expiration details, and barcodes including the NDC code 0002-3251-30.*

* 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.