Doxepin Tablet
Product Images NDC 59651-845

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Doxepin (NDC 59651-845). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurobindo Pharma Limited, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Package Label-principal Display Panel (3 mg (30 Tablets Bottle))

Package Label-principal Display Panel (3 mg (30 Tablets Bottle))
Label for Doxepin Tablets 3 mg oral tablets by Aurobindo Pharma Limited. The label shows the NDC 59651-844-30, a 30-tablet package, and contains dosing information noting each tablet contains 3 mg doxepin. It includes storage instructions, distributor details for Aurobindo Pharma USA, and pharmacy dispensing guidance.*
FDA Label Image

Package Label-principal Display Panel (6 mg (30 Tablets Bottle))

Package Label-principal Display Panel (6 mg (30 Tablets Bottle))
Doxepin Tablets 6 mg oral tablets label shows the product NDC 59651-845-30, containing 6 mg of doxepin per tablet. The label states a quantity of 30 tablets, distributed by Aurobindo Pharma USA, Inc. The packaging includes storage instructions at 20° to 25°C and dispensing guidelines for pharmacists. It shows the labeler as Aurobindo Pharma Limited and includes a barcode.*
FDA Label Image

Chemical Structure (Doxepin Str)

Chemical Structure (Doxepin Str)
Chemical structure diagram of doxepin hydrochloride, showing its molecular framework with aromatic rings and functional groups as labeled in the image.*

* 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.