Paroxetine
Product Images NDC 70934-661

2 FDA label images from Denton Pharma, Inc. Dba Northwind Pharmaceuticals · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Paroxetine (NDC 70934-661). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Denton Pharma, Inc. Dba Northwind Pharmaceuticals, 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

Label (70934 661 30 Master Bottle Label Approval Rev A 04 20)

Label (70934 661 30 Master Bottle Label Approval   Rev A 04 20)
Paroxetine Tablets, USP 20mg label from Denton Pharma, Inc. dba Northwind Pharmaceuticals featuring 30 tablets per container. The label includes storage instructions, dosage instructions referencing the package insert, and multiple identical secondary labels with lot, NDC, and expiration date placeholders. The main label also states the product is for prescription use only and cautions to keep out of reach of children.*
FDA Label Image

Structured Formula For Paroxetine (Eb2eb1e9 4c97 4349 8895 019684561a2b 01)

Structured Formula For Paroxetine (Eb2eb1e9 4c97 4349 8895 019684561a2b 01)
Chemical structure diagram of the active ingredient Paroxetine hydrochloride, showing its molecular arrangement with labeled atoms and bonds.*

* 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.