Venlafaxine
Product Images NDC 53217-238

3 FDA label images from Aidarex Pharmaceuticals Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Venlafaxine (NDC 53217-238). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aidarex Pharmaceuticals Llc, 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

Venlafaxine-figure-1 (Venlafaxine Usp 1)

Venlafaxine-figure-1 (Venlafaxine Usp 1)
Chemical structure of Venlafaxine hydrochloride, depicting the molecular arrangement of atoms including a methoxyphenyl group, cyclohexanol moiety, and a dimethylaminoethyl side chain.*
FDA Label Image

Image Label (Venlafaxine Usp 2)

Image Label (Venlafaxine Usp 2)
Venlafaxine, USP 37.5 mg tablets in a 30 count package. The label shows the active ingredient as venlafaxine hydrochloride equivalent to venlafaxine base 37.5 mg. It is a peach pentagon-shaped tablet with a score on the reverse side. Manufactured by Alkaloida Chemical Company ZRT, Hungary, and packaged by Aidarex Pharmaceuticals LLC. The label includes NDC 53217-0218-30 and dosage instructions space.*
FDA Label Image

Package Label (Venlafaxine Usp 3)

Package Label (Venlafaxine Usp 3)
Venlafaxine USP 50 mg tablet packaging label shows 60 tablets per package. The label states the active ingredient Venlafaxine Hydrochloride equivalent to Venlafaxine base 50 mg. It is a Peach Pentagon tablet with scoring on one side and reverse. The label identifies Aidarex Pharmaceuticals LLC as the packager and Alkaloida Chemical Company ZRT. Hungary as the manufacturer. It includes NDC 53217-0238-60 and space for lot and usage 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.