Venlafaxine Hydrochloride Capsule, Extended Release
Product Images NDC 68788-7919

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Venlafaxine Hydrochloride (NDC 68788-7919). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Preferred Pharmaceuticals 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

Figure 1: Effect Of Interacting Drugs On The Pharmacokinetics Of Venlafaxine And Active Metabolite O-desmethylvenlafaxine (odv). (Venlafaxine Fig1)

FDA Label Image

Figure 2: Effect Of Venlafaxine On The Pharmacokinetics Interacting Drugs And Their Active Metabolites. (Venlafaxine Fig2)

FDA Label Image

Figure 3: Pharmacokinetics Of Venlafaxine And Its Metabolite O-desmethylvenlafaxine (odv) In Special Populations. (Venlafaxine Fig3)

FDA Label Image

Venlafaxine HCl Extended-release Capsules 37.5mg (Venlafaxine Fig4)

Venlafaxine HCl Extended-release Capsules 37.5mg (Venlafaxine Fig4)
This is a description of Venlafaxine HCI Extended-Release Capsules 37.5mg, a generic version of Effexor ER. The capsules contain Venlafine Eydrochlonde et 37.5 mg of Venlafasine. The Pl Size, Exp Date, Lot#, Batch#, Ins, and Mfg (Aurobindo Pharma Limited) are also mentioned. There are directions for use in both English and Spanish, cautionary notes about transferring the drug to others, and insurance details.*
FDA Label Image

Chemical Structure (Venlafaxine Str)

* 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.