Paroxetine Tablet, Film Coated
Product Images NDC 70518-2574

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Paroxetine (NDC 70518-2574). 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 10mg 70518 2574 01

Paroxetine 10 mg film-coated tablets packaging label showing a quantity of 30 tablets. The label includes the NDC number 70518-2574-01 and states the product is repackaged by RemedyRepack Inc., Indiana, PA. Manufacturer is Aurobindo Pharma, Dayton, NJ. Storage instructions specify 20-25°C with permitted excursions and a reminder to keep medication out of reach of children.*

FDA Label Image

Paroxetine 10mg 70518 2574 02

Paroxetine 10 mg tablet label displaying the dosage strength and quantity of 1 tablet. The label includes manufacturer information, a QR code, and storage directions. The product is repackaged by RemedyRepack Inc., with reference to source manufacturer Aurobindo Pharma. The label states 'RX ONLY' and advises keeping medication out of children's reach.*

FDA Label Image

Remedy_label (Remedy Label)

Paroxetine 10 mg tablet label showing the quantity of 90 tablets. The label includes the NDC number 70518-2574-00, repackaged by RemedyRepack Inc., Indiana, PA, with directions to see the package insert. Manufacturer information shows Aurobindo Pharma in Dayton, NJ. Storage instructions and a QR code are also visible.*

FDA Label Image

Paroxetine Fig1

Chemical structure diagram of paroxetine hydrochloride, showing its molecular ring components including fluorophenyl, piperidine, and methylenedioxy groups.*

* 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.