Venlafaxine Hydrochloride Tablet, Extended Release
Product Images NDC 47335-758

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 47335-758). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, 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

Spl-venlafaxine-lable-1 (Spl Venlafaxine Lable 1)

Spl-venlafaxine-lable-1 (Spl Venlafaxine Lable 1)
Label for Venlafaxine Hydrochloride Extended-Release Tablets, 37.5 mg strength, oral extended-release tablets. The label indicates a package size of 30 tablets and is manufactured by Sun Pharmaceutical Industries, Inc. It includes a barcode and instructions for pharmacists to dispense with a medication guide.*
FDA Label Image

Spl-venlafaxine-lable-2 (Spl Venlafaxine Lable 2)

Spl-venlafaxine-lable-2 (Spl Venlafaxine Lable 2)
Label for Venlafaxine Hydrochloride Extended-Release Tablets 75 mg by Sun Pharmaceutical Industries, Inc. The label indicates a 30-tablet prescription-only package and instructs pharmacists to dispense with the medication guide. The NDC code and barcode are also visible.*
FDA Label Image

Spl-venlafaxine-lable-3 (Spl Venlafaxine Lable 3)

Spl-venlafaxine-lable-3 (Spl Venlafaxine Lable 3)
Label for Venlafaxine Hydrochloride Extended-Release Tablets 150 mg by Sun Pharmaceutical Industries, Inc. The label includes the strength 150 mg, indicates the dosage form as extended-release tablets, and shows the package contains 30 tablets. It is marked Rx only and instructs pharmacists to dispense with the medication guide.*
FDA Label Image

Spl Venlafaxine Lable 4

Spl Venlafaxine Lable 4
Label for Venlafaxine Hydrochloride Extended-Release Tablets 225 mg, a human prescription oral tablet by Sun Pharmaceutical Industries, Inc. The label states the dosage strength as 225 mg and that the package contains 30 tablets. It includes storage instructions, dosage guidance, a barcode, distributor and manufacturer details, and the Sun Pharma logo.*
FDA Label Image

Venlafaxine-str (Venlafaxine Str)

Venlafaxine-str (Venlafaxine Str)
Chemical structure of venlafaxine hydrochloride showing its molecular framework with functional groups including a methoxy-substituted aromatic ring, a cyclic structure, and dimethylamine moiety.*

* 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.