Atomoxetine Capsule
Product Images NDC 0093-3542

9 FDA label images from Teva Pharmaceuticals Usa, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Atomoxetine (NDC 0093-3542). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Teva Pharmaceuticals Usa, Inc., 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 1

Image 1
Two line charts showing the mean weight percentile and mean height percentile over 36 months of treatment. The left chart presents mean weight percentile data for 203 subjects, indicating an initial decrease followed by a gradual increase. The right chart shows mean height percentile data for 155 subjects, remaining relatively stable with minor fluctuations over time.*
FDA Label Image

Image 2

Image 2
Chemical structure of Atomoxetine hydrochloride, showing its molecular components including a methylated aromatic ring, an ether linkage, and an amine group with hydrochloride salt.*
FDA Label Image

Image 3

Image 3
Label for Atomoxetine Capsules, USP, 10 mg strength, oral capsules by Teva Pharmaceuticals USA, Inc. The label indicates a 30 capsule package, prescription use only, with instructions for pharmacists to dispense the Medication Guide. The label includes an NDC number 0093-3542-56 and highlights a tamper-evident closure and child-resistant container warnings.*
FDA Label Image

Image 4

Image 4
Label for Atomoxetine Capsules, USP 18 mg by Teva Pharmaceuticals USA, Inc. The label shows the NDC 0093-3543-56, specifies 18 mg strength, oral capsule dosage form, and a package size of 30 capsules. It includes dispensing instructions for pharmacists and storage information. The Teva logo is shown in green at the bottom right.*
FDA Label Image

Image 5

Image 5
Label for Atomoxetine Capsules, USP 25 mg by Teva Pharmaceuticals USA, Inc. The label includes NDC 0093-3544-56, a barcode, and instructions to dispense the Medication Guide. It specifies that the package contains 30 capsules for oral use and is Rx only.*
FDA Label Image

Image 6

Image 6
Label for Atomoxetine Capsules, USP 40 mg by Teva Pharmaceuticals USA, Inc., showing prescription medication information. The label indicates a package of 30 capsules, with instructions for pharmacists to dispense the Medication Guide. The NDC number 0093-3545-56 and a barcode are present, along with storage and safety instructions, including keeping out of reach of children and storing at 20° to 25°C.*
FDA Label Image

Image 7

Image 7
Label for Atomoxetine Capsules, USP 60 mg oral capsules by Teva Pharmaceuticals USA, Inc. The bottle contains 30 capsules and is marked Rx only. The label includes handling instructions, storage conditions, and a serialization coding area. It also mentions dispensing the accompanying Medication Guide to each patient.*
FDA Label Image

Image 8

Image 8
Label for Atomoxetine Capsules, USP 80 mg oral capsules by Teva Pharmaceuticals USA, Inc. The package contains 30 capsules and is labeled for prescription use only. Label includes storage instructions, cautionary warnings against use in children, and a barcode. The NDC code is 0093-3547-56.*
FDA Label Image

Image 9

Image 9
The label for Atomoxetine Capsules, USP, 100 mg strength, in a 30 capsule bottle format by Teva Pharmaceuticals USA, Inc. It includes dosage instructions, a barcode, serialization coding area, and the National Drug Code (NDC) 0093-3548-56. Safety warnings and storage information are also visible.*

* 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.