Strattera Capsule
Product Images NDC 0002-3229

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Strattera (NDC 0002-3229). 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

Package Label (STRATTERA 100 mg bottle of 30)

Strattera 100 mg capsules label by Eli Lilly and Company. The label shows the product name, active ingredient Atomoxetine capsules, strength 100 mg, and quantity 30 capsules. It includes dosing information, a barcode, a capsule image, and instructions to not use if the tamper-evident seal is broken, with a website reference at www.strattera.com.*

FDA Label Image

Package Label (STRATTERA 10 mg bottle of 30)

Strattera 10 mg atomoxetine capsules label showing a 30-capsule package from Eli Lilly and Company. The label includes dosage strength, dispensing instructions, storage conditions, barcode, and warnings about capsule integrity. The label is primarily white with gold and purple accents and features the Eli Lilly logo.*

FDA Label Image

Package Label (STRATTERA 18 mg bottle of 30)

Strattera 18 mg capsules packaging label by Eli Lilly and Company. The label shows the product name and generic name Atomoxetine capsules, strength of 18 mg, and a quantity of 30 capsules. It also includes medication guidance, storage instructions, a barcode, NDC 0002-3238-30, and a caution about using the package if the inner seal is missing or broken.*

FDA Label Image

Package Label (STRATTERA 25 mg bottle of 30)

Label for Strattera 25 mg capsules showing the brand name and generic name Atomoxetine capsules. The label specifies prescription-only status, capsule count of 30, and NDC code 0002-3228-30. It includes manufacturer Eli Lilly and Company and highlights a warning about not using if the inner seal is broken. A barcode and storage instructions are also visible.*

FDA Label Image

Package Label (STRATTERA 40 mg bottle of 30)

Label for Strattera 40 mg oral capsules by Eli Lilly and Company. The label specifies atomoxetine hydrochloride as the active ingredient, with 30 capsules per container. It includes storage instructions, a warning to not use if the inner seal is missing or broken, and a medication guide notice. A barcode and NDC number 0002-3229-30 are also present.*

FDA Label Image

Package Label (STRATTERA 60 mg bottle of 30)

Label for Strattera 60 mg capsules, containing atomoxetine hydrochloride, for oral use. The label indicates prescription-only status and states each capsule is equivalent to 60 mg atomoxetine. It includes a warning not to use if the Eli Lilly inner seal is missing or broken and provides storage instructions. The label shows the NDC 0002-3239-30 and manufacturer Eli Lilly and Company.*

FDA Label Image

Package Label (STRATTERA 80 mg bottle of 30)

Strattera 80 mg atomoxetine capsules label from Eli Lilly and Company. The label indicates the product contains 30 capsules with each capsule equivalent to 80 mg atomoxetine. Includes warning to not use if the Lilly inner seal is missing or broken, storage instructions, RX only designation, and a barcode.*

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

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.*

* 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.