Venlafaxine Tablet
Product Images NDC 70518-1385

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Venlafaxine (NDC 70518-1385). 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

Mm1 (Venlafaxine 37.5mg 70518 1385 00)

Venlafaxine 37.5 mg tablet label showing a quantity of 30 tablets. The label indicates it is prescription only, with NDC 70518-1385-00, manufactured by Rising Pharma, Inc., Allendale, NJ. It also mentions repackaging by RemedyRepack Inc., Indiana, PA, and includes storage instructions and a QR code.*

FDA Label Image

Mm2 (Venlafaxine 37.5mg 70518 1385 01)

Label for venlafaxine 37.5 mg oral tablets, quantity 90, repackaged by RemedyRepack Inc. The label indicates Rx only status, includes NDC 70518-1385-01, and notes manufacturing by Rising Pharma, Inc., Allendale, NJ. Storage instructions and a QR code are also visible.*

FDA Label Image

Mm3 (Venlafaxine 37.5mg 70518 1385 02)

Label for venlafaxine 37.5 mg oral tablet, quantity 30, labeled by RemedyRepack Inc. It includes the NDC number 70518-1385-02 and manufacturer Rising Pharma, Inc. Directions refer to the package insert with storage instructions at 20-25°C. The label also includes a barcode and a QR code.*

FDA Label Image

Chemical Structure (Venlafaxine Str)

Chemical structure of venlafaxine hydrochloride, showing the molecular arrangement with a cyclohexane ring, a methoxy-substituted benzene ring, and an ethanolamine side chain including a dimethylamino group, labeled with the hydrochloride salt.*

* 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.