Armodafinil Tablet
Product Images NDC 0093-3092

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

Product Visual Gallery

This gallery contains 13 technical images submitted to the FDA as part of the official labeling for Armodafinil (NDC 0093-3092). 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

FDA Label Image

Armodafinil Tablets Civ 150 mg, 30s Label (Image 10)

Armodafinil Tablets Civ 150 mg, 30s Label (Image 10)
Label for Armodafinil Tablets 50 mg by Teva Pharmaceuticals USA, Inc. The label indicates each tablet contains 50 mg armodafinil and includes a note on medication guide requirements and dispensing instructions. The package contains 30 tablets, with the NDC 0093-3090-56 and a revision date of 3/2017 visible.*
FDA Label Image

Armodafinil Tablets Civ 200 mg, 30s Label (Image 11)

Armodafinil Tablets Civ 200 mg, 30s Label (Image 11)
Armodafinil 150 mg tablets packaging label by Teva Pharmaceuticals USA, Inc. The label identifies 30 tablets per package, including a NDC code 0093-3092-56, and notes prescription use only. The label includes serialization coding and manufacturing details.*
FDA Label Image

Armodafinil Tablets Civ 250 mg, 30s Label (Image 12)

Armodafinil Tablets Civ 250 mg, 30s Label (Image 12)
Label for Armodafinil Tablets 200 mg by Teva Pharmaceuticals USA, Inc. The label states prescription use, packaging of 30 tablets, and includes a serialized coding area, NDC number 0093-3093-56, and bar code. It includes a warning that each tablet contains 200 mg armodafinil.*
FDA Label Image

Image 13

Image 13
Label for Armodafinil Tablets 250 mg by Teva Pharmaceuticals USA, Inc. The label indicates a package containing 30 tablets. It includes a Medication Guide requirement and states the product is Rx only. The label features the NDC number 0093-3094-56 and revision date 3/2017.*
FDA Label Image

Image 2

FDA Label Image

Image 3

FDA Label Image

Image 4

FDA Label Image

Image 5

Image 5
Chemical structure of the active ingredient Armodafinil.*
FDA Label Image

Image 6

FDA Label Image

Image 7

FDA Label Image

Image 8

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Image 9

* 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.