Venlafaxine Hydrochloride
Product Images NDC 68025-081

Product Visual Gallery

This gallery contains 11 technical images submitted to the FDA as part of the official labeling for Venlafaxine Hydrochloride (NDC 68025-081). 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)

FDA Label Image

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

Venlafaxine Extended Release Tablets are a prescription medicine that comes in 225mg tablets. It contains venlafaxine hydrochloride. It is important to always provide the attached Medication Guide to patients when dispensing these tablets. *

FDA Label Image

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

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)

This is a description for Venlafaxine extended release tablets with NDC number 68025-079-30. Each tablet has a potency equivalent to 37.5mg of venlafaxine and is dispensed in unit doses with an attached medication guide. The recommended dosage is once a day, and the tablets should be stored at temperatures between 25°C to 30°C, protected from moisture and humidity. This medication is only available with a prescription.*

FDA Label Image

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

This text appears to be a medication package for Venlafaxine extended-release tablets. Each tablet contains 37.5 mg of Venlafaxine and is intended for daily use. The medication is only available with a prescription (Rx only). The package includes an attached medication guide and should be stored at room temperature (25°C/77°F) with limited excursions. Further details can be found in the package insert.*

FDA Label Image

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

This is a medication package for Venlafaxine Extended Release Tablets. It contains 30 tablets, each containing a dosage of 75 mg of Venlafaxine. The usual dosage is once per day. The medication guide should be attached to every pack of this medication. It can be stored at a temperature between 25°C to 30°C.*

FDA Label Image

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

This is a description of a medication called V1988002, which is a Unit of Use that contains 90 extended-release tablets of the drug Venlafaxine. The tablets are only available with a prescription and it is recommended to give the patient the attached Medication Guide. Each tablet has a dosage of 75mg and is intended to be taken once daily. The medication should be protected from moisture and harmful elements.*

FDA Label Image

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

This is a prescription drug with the name Venlafaxine. It is an extended-release tablet available in 30 units of use. It is important that each time this drug is dispensed, the patient receives a medication guide attached to the medication.*

FDA Label Image

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

This is a description for Venlafaxine Extended Release Tablets medication. It contains 90 tablets, and each tablet has an equivalent of 150 mg of venlafaxine in an extended-release formulation. It is advised to give the patients the attached Medication Guide before dispensing the tablets. The usual dosage is once daily, and more information about dosage can be found on the package insert. The medication is for prescription-only, and it is allowed to have excursions to the USP Controlled Room.*

* 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.