Paroxetine Tablet, Film Coated
Product Images NDC 70518-1460

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Paroxetine (NDC 70518-1460). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack 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

Paroxetine 30mg 70518 1460 00

Label for PARoxetine 30 mg film-coated tablets, quantity of 90, repackaged by RemedyRepack Inc. The label includes the NDC number 70518-1460-00, manufacturer Apotex Corp. in Weston, FL, and storage instructions. It specifies prescription use only and advises to keep out of reach of children.*

FDA Label Image

Paroxetine 30mg 70518 1460 01

Label for PARoxetine 30 mg film-coated tablets, quantity of 100, repackaged by RemedyRepack Inc. The label includes the NDC number 70518-1460-01, manufacturer Apotex Corp., and storage instructions (20-25°C, excursions 15-30°C). The label directs users to see the package insert for directions.*

FDA Label Image

Paroxetine 30mg 70518 1460 02

PAROXETINE 30 mg film-coated tablet label showing prescription status, quantity of 1 tablet, and manufacturer information. The label includes the product NDC 70518-1460-02 and indicates repackaging by RemedyRepack Inc. Directions reference the package insert for use. Storage conditions are also provided.*

* 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.