Venlafaxine Hydrochloride
Product Images NDC 68025-082

Product Visual Gallery

This gallery contains 11 technical images submitted to the FDA as part of the official labeling for Venlafaxine Hydrochloride (NDC 68025-082). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Vertical 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

Structural Formula (Venlafaxine Extended Release Tablets 1)

Chemical structure of venlafaxine hydrochloride, showing the molecular arrangement including a methoxy-substituted aromatic ring, a cyclohexane ring, and a dimethylamine group.*

FDA Label Image

Vertical 225mg 30ct (Venlafaxine Extended Release Tablets 10)

Label for Venlafaxine Extended Release Tablets 225 mg, containing venlafaxine hydrochloride as the active ingredient, marketed by Vertical Pharmaceuticals, LLC. The label includes NDC 68025-082-30 and specifies a 30-tablet unit of use. Dosage information and storage instructions are also visible.*

FDA Label Image

Vertical 225mg 90ct (Venlafaxine Extended Release Tablets 11)

Label for Venlafaxine Extended Release Tablets by Vertical Pharmaceuticals, LLC, indicating 225 mg strength per tablet as venlafaxine hydrochloride. The label states Rx Only, includes dosing information, storage instructions, and a 90-tablet unit of use. Barcode and revision date (10/2016) are visible.*

FDA Label Image

Vertical Logo (Venlafaxine Extended Release Tablets 2)

FDA Label Image

Vertical Logo (Venlafaxine Extended Release Tablets 3)

FDA Label Image

Vertical 37.5mg 30ct (Venlafaxine Extended Release Tablets 4)

Label for Venlafaxine Extended Release Tablets containing 37.5 mg of venlafaxine hydrochloride per tablet. The label states the dosage form as extended release tablets and the unit of use package contains 30 tablets. It is marked by Vertical Pharmaceuticals, LLC, and includes storage instructions and dispensing notes.*

FDA Label Image

Vertical 37.5mg 90ct (Venlafaxine Extended Release Tablets 5)

Venlafaxine Extended Release Tablets 37.5 mg (venlafaxine hydrochloride) label showing dose strength, instructions for dispenser, storage conditions, package size of 90 tablets, and manufacturer listed as Vertical Pharmaceuticals, LLC. The label includes NDC code 68025-079-90 and barcode.*

FDA Label Image

Vertical 75mg 30ct (Venlafaxine Extended Release Tablets 6)

Venlafaxine Hydrochloride Extended Release Tablets 75 mg label from Vertical Pharmaceuticals, LLC. The label displays the product name, strength, dosage form, and manufacturer details. It includes usage instructions, storage conditions, and NDC code 68025-080-30. The package contains 30 tablets intended for prescription use only.*

FDA Label Image

Vertical 75mg 90ct (Venlafaxine Extended Release Tablets 7)

Venlafaxine Extended Release Tablets 75 mg, containing venlafaxine hydrochloride, marketed by Vertical Pharmaceuticals, LLC. The label states the strength as 75 mg per tablet and includes dispensing instructions, package size of 90 tablets, storage conditions, and a medication guide note for authorized dispensers. A barcode and NDC 68025-080-90 are visible.*

FDA Label Image

Vertical 150mg 30ct (Venlafaxine Extended Release Tablets 8)

Label for Venlafaxine Extended Release Tablets by Vertical Pharmaceuticals, LLC. The label indicates the active ingredient is venlafaxine hydrochloride with a strength of 150 mg per tablet. The package contains 30 tablets and is designated Rx Only. Directions mention the usual adult dose and storage requirements.*

FDA Label Image

Vertical 150mg 90ct (Venlafaxine Extended Release Tablets 9)

Venlafaxine Extended Release Tablets label showing 150 mg strength of venlafaxine hydrochloride. The label includes dosage instructions, storage conditions, a barcode, and states the package contains 90 tablets. Marketed by Vertical Pharmaceuticals, LLC.*

* 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.