Venlafaxine Tablet
Product Images NDC 68084-856

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Venlafaxine (NDC 68084-856). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by American Health Packaging, 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

Ahp89625

Venlafaxine 37.5 mg round oral tablets imprinted with "ZC" over "64" on one side and plain on the other. The tablets are light beige and uncoated, manufactured by American Health Packaging.*

FDA Label Image

Ahp84401

Venlafaxine 75 mg oral tablet by American Health Packaging, shown front and back. The front side has an imprint 'ZC 65' with a score line; the back is plain. The round tablet is beige and measures approximately 9 mm in diameter.*

FDA Label Image

Ahp85601

Venlafaxine 75 mg oral tablets by American Health Packaging shown. One round, light-colored tablet is scored with imprint 'ZC 67' on one side and plain on the other. Tablets are prescription human drugs used in oral dosage form.*

FDA Label Image

Structural Formula (Structure)

Chemical structure of Venlafaxine hydrochloride, showing the molecular arrangement including a cyclohexane ring, a methoxy-substituted phenyl ring, a hydroxyl group, and a dimethylaminoethyl side chain.*

FDA Label Image

25 mg Venlafaxine Tablets Carton (25 mg Carton)

Venlafaxine Tablets USP 25 mg oral tablet label shows a 30-tablet count (5 x 6) from American Health Packaging. The label includes dosage strength, NDC number 68084-896-25, and dispensing instructions with warnings and storage conditions. The product is marked Rx Only and is distributed by American Health Packaging, Columbus, Ohio.*

FDA Label Image

25 mg Venlafaxine Tablet Blister (25 mg Blister)

Venlafaxine 25 mg oral tablets packaging label from American Health Packaging. The label displays the drug name, strength, dosage form, lot number 123456, and expiry date 08/15. The label is designed for a carton or blister pack with barcode and company address in Columbus, OH.*

FDA Label Image

37.5 mg Venlafaxine Tablets Carton (37.5 mg Carton.jpg)

Venlafaxine Tablets USP 37.5 mg oral tablets, packaged as 100 tablets (10 x 10) by American Health Packaging. The label includes NDC 68084-844-01, barcode, dosing information, storage instructions, and a QR code for medication guide and prescribing information. The product is Rx only and distributed by American Health Packaging, Columbus, Ohio.*

FDA Label Image

37.5 mg Venlafaxine Tablet Blister (37.5 mg Blister.jpg)

A blister card label for Venlafaxine tablets, USP 37.5 mg by American Health Packaging. The label shows repeated sections containing the product name, dosage form, strength, lot number 123456, and expiration date 01/16. It includes a barcode and NDC 0054-0647-17, indicating oral tablet dosage form.*

FDA Label Image

75 mg Venlafaxine Tablets Carton (600 mg Carton)

Venlafaxine Tablets, USP 75 mg oral tablets in a package containing 100 tablets (10 blister packs of 10). Label displays the NDC 68084-856-01 and indicates the product is Rx only. The label includes dosing information, storage conditions, and a QR code for medication guide and prescribing information. Distributed by American Health Packaging.*

FDA Label Image

75 mg Venlafaxine Tablet Blister (75 mg Blister)

Venlafaxine 75 mg oral tablets labels from American Health Packaging. The image shows multiple identical rectangular labels displaying the drug name, dosage strength, route, and a barcode, with space for lot number and expiration date information. Each label includes the manufacturer's location in Columbus, Ohio.*

* 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.