Venlafaxine Hydrochloride
Product Images NDC 13811-714

Product Visual Gallery

This gallery contains 11 technical images submitted to the FDA as part of the official labeling for Venlafaxine Hydrochloride (NDC 13811-714). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Trigen Laboratories, 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 its molecular components including a cyclohexane ring, a methoxyphenyl group, and a dimethylamino group with the hydrochloride salt indicated.*

FDA Label Image

225mg 30ct (Venlafaxine Extended Release Tablets 10)

Label for Venlafaxine Extended Release Tablets 225 mg by Trigen Laboratories, LLC. The label shows dosage strength as 225 mg, mentions extended release formulation, usual dosage once daily, storage instructions at controlled room temperature, and package contains 30 tablets.*

FDA Label Image

225mg 90ct (Venlafaxine Extended Release Tablets 11)

Label for Venlafaxine Extended Release Tablets 225 mg, containing venlafaxine hydrochloride. The label indicates an extended release formulation with a unit of use containing 90 tablets. It is marketed by Trigen Laboratories, LLC with storage instructions and usage guidance noted on the label.*

FDA Label Image

Trigen Logo (Venlafaxine Extended Release Tablets 2)

FDA Label Image

Trigen Logo (Venlafaxine Extended Release Tablets 3)

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37.5mg 30ct (Venlafaxine Extended Release Tablets 4)

Label for Venlafaxine Hydrochloride Extended Release Tablets, 37.5 mg strength, marketed by Trigen Laboratories, LLC. The label indicates a unit of use with 30 tablets and includes usage instructions, storage conditions at 25°C (77°F) with allowable excursions, and a note to authorized dispensers to provide the medication guide with each dispense. The NDC number 13811-712-30 is also shown.*

FDA Label Image

37.5mg 90ct (Venlafaxine Extended Release Tablets 5)

Label for Venlafaxine Hydrochloride Extended Release Tablets 37.5 mg by Trigen Laboratories, LLC. The label states each tablet contains 37.5 mg venlafaxine in extended release formulation. The unit of use is 90 tablets. The label includes storage instructions and dosing guidance for once daily use.*

FDA Label Image

75mg30ct (Venlafaxine Extended Release Tablets 6)

Label for Venlafaxine Hydrochloride Extended Release Tablets, 75 mg strength, marketed by Trigen Laboratories, LLC. The label indicates the unit of use contains 30 tablets, with storage instructions at 25°C (77°F) and protecting from moisture and humidity. The label also notes dispensing instructions and lists the NDC 13811-713-30.*

FDA Label Image

75mg 90ct (Venlafaxine Extended Release Tablets 7)

Label for Venlafaxine Extended Release Tablets 75 mg, marketed by Trigen Laboratories, LLC. The label states each tablet contains 75 mg of venlafaxine hydrochloride in an extended release formulation. It indicates the usual dosage as once daily and provides storage instructions to keep at 25°C (77°F), protecting from moisture and humidity. The package contains 90 tablets.*

FDA Label Image

150mg 30ct (Venlafaxine Extended Release Tablets 8)

Label for Venlafaxine Extended Release Tablets, 150 mg strength as venlafaxine hydrochloride. The label indicates the product is marketed by Trigen Laboratories, LLC and has an NDC number 13811-714-30. It includes storage instructions, dosage direction, barcode, and notes for the authorized dispenser. The package contains 30 tablets.*

FDA Label Image

150mg 90ct (Venlafaxine Extended Release Tablets 9)

Label for Venlafaxine Extended Release Tablets (venlafaxine hydrochloride) 150 mg, marketed by Trigen Laboratories, LLC. The label notes 90 tablets per unit, with instructions for storage at 25°C (77°F) and dosage directions indicating once daily use. The NDC number 13811-714-90 is shown along with warnings to protect from moisture and humidity.*

* 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.