Venlafaxine Hydrochloride
Product Images NDC 61919-920

3 FDA label images from Direct Rx · 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 Hydrochloride (NDC 61919-920). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Direct Rx, 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

Image Description (Label 2)

Image Description (Label 2)
VENLAFAXINE 75mg 90 tablets label for generic Effexor, packaged and distributed by Direct Rx. The label includes warnings to keep out of reach of children, storage instructions, NDC 61919-535-90, lot and expiration date information, and manufacturer details (Mfg NDC 23155-249-01).*
FDA Label Image

Image Description (Label)

Image Description (Label)
VENLAFAXINE 75 mg, 30 tablets. Generic for EFFEXOR, each tablet contains Venlafaxine hydrochloride USP equivalent to 75 mg of venlafaxine. Packaged and distributed by DIRECT RX, Alpharetta, GA. The label includes warnings about drowsiness or dizziness and instructs that medication should be taken with food. Barcode and lot numbers are present, along with discard instructions dated 01/18.*
FDA Label Image

Image Description (Molecule)

Image Description (Molecule)
Chemical structure of venlafaxine hydrochloride depicted as a molecular diagram with labeled chemical groups and a hydrochloride component, corresponding to the active ingredient venlafaxine hydrochloride.*

* 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.