Paroxetine
Product Images NDC 61919-658

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Paroxetine (NDC 61919-658). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Direct Rx, 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

61919 0658 60

Packaging label for Paroxetine 20 mg tablets, displaying quantity of 60 tablets. It states that Paroxetine is a generic for Paxil and that each tablet contains Paroxetine hydrochloride equivalent to 20 mg paroxetine. The label includes lot number, expiry date (12/31/21), and indicates packaging and distribution by Direct Rx.*

FDA Label Image

658 30

Packaging label for Paroxetine 20mg tablets, containing 30 tablets per bottle. The label states it is a generic for Paxil and lists paroxetine hydrochloride as the active ingredient equivalent to 20mg paroxetine per tablet. Labeler is Direct RX, with packaging location Alpharetta, GA. The label includes lot number, expiration date (02/20), and multiple NDC codes and barcodes.*

FDA Label Image

Image Description (Module)

Chemical structure of paroxetine hydrochloride, illustrating its molecular framework including a fluorophenyl ring, piperidine ring, and a lactone-containing bicyclic moiety.*

FDA Label Image

Label (Paroxetine322)

Paroxetine 10mg tablet bottle label showing 30 tablets, generic for Paxil, labeled by Direct Rx. The label includes dosage information, lot number (Prod# 322-30), expiration date (05/17), and manufacturer location in Alpharetta, GA. Drug and safety warnings indicate prescription-only status and storage instructions.*

* 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.