Doxepin Tablet, Film Coated
Product Images NDC 0228-3316

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Doxepin (NDC 0228-3316). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Actavis Pharma, 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

T:\maryland\nj\chris\doxepin Tablets, 3 mg & 6 mg\a1.jpg (Image 1)

Label for Doxepin tablets, film-coated, available in strengths of 3 mg and 6 mg. The label includes the generic name Doxepin and indicates the dosage form as film-coated tablets. The labeler is Actavis Pharma, Inc. The image shows two different tablets side by side, one white and one pink, each marked with alphanumeric codes.*

FDA Label Image

5c3be85e-figure-02 (Image 2)

Chemical structure diagram of doxepin, showing its tricyclic ring structure and attached side chains, as part of the drug's molecular representation.*

FDA Label Image

5c3be85e-figure-03 (Image 3)

FDA Label Image

5c3be85e-figure-04 (Image 4)

FDA Label Image

Label 3 mg (Image 5)

Doxepin Tablets 3 mg film-coated tablets label displaying a package size of 30 tablets. The label includes dispensing instructions, storage conditions, manufacturer information (Teva Pharmaceuticals USA, Inc.), and a barcode. The strength is prominently noted in a green box on the left side of the label.*

FDA Label Image

Label 6 mg (Image 6)

Label for Doxepin Tablets 6 mg, film-coated tablets in a package of 30. The label shows storage instructions, dosage form, strength, and manufacturer information (Teva Pharmaceuticals USA, Inc.). It includes NDC 0228-3316-03 and a barcode.*

* 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.