Paroxetine Tablet, Film Coated
Product Images NDC 70518-2387

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Paroxetine (NDC 70518-2387). 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

Structured Formula For Paroxetine (6cfde064 Ddcb 49df A53c 953c40eb1470 01)

Chemical structure of paroxetine hydrochloride hemihydrate showing the molecular arrangement with a fluorophenyl group attached to a piperidine ring and associated hydrochloride salt.*

FDA Label Image

Mm3 (Paroxetine 20mg 70518 2387 01)

Paroxetine 20 mg film-coated tablet single unit packaging label by RemedyRepack Inc. The label includes NDC number 70518-2387-01, indicates it is prescription only (RX ONLY), and notes the repackaging source and storage conditions.*

FDA Label Image

Paroxetine 20mg 70518 2387 02

Paroxetine 20 mg film-coated tablets label showing a quantity of 30 tablets. The label includes the proprietary name Paroxetine and highlights the 20 mg strength. It is labeled for oral use and prescription only (RX ONLY) by RemedyRepack Inc. Additional information includes an NDC number, manufacturer details, storage instructions, and a QR code.*

FDA Label Image

Paroxetine 20mg 70518 2387 03

Paroxetine 20 mg tablet packaging label showing a single oral film-coated tablet. The label displays the proprietary name Paroxetine, strength 20 mg, and quantity 1 tablet. The product is labeled as Rx only, repackaged by RemedyRepack Inc. The label includes NDC 70518-2387-03, manufacturing information, and storage conditions.*

FDA Label Image

Remedy_label (Remedy Label)

Paroxetine 20 mg film-coated tablets label shows a quantity of 30 tablets. The label includes the NDC number 70518-2387-00 and states the medication is repackaged by RemedyRepack Inc. Directions advise referencing the package insert. Storage instructions specify 20-25°C with permitted excursions. Manufacturer Solco, Cranbury, NJ is noted.*

* 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.