Effexor
Product Images NDC 21695-046

5 FDA label images from Rebel Distributors Corp · 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 Effexor (NDC 21695-046). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rebel Distributors Corp, 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

Chemical Structure (8a2302ca 5c25 4d2d 9ffe 320080934aab 01)

Chemical Structure (8a2302ca 5c25 4d2d 9ffe 320080934aab 01)
Chemical structure diagram of venlafaxine hydrochloride, the active ingredient in Effexor XR Extended-Release.*
FDA Label Image

Computer_2.jpg (8a2302ca 5c25 4d2d 9ffe 320080934aab 02)

FDA Label Image

Phone_2.jpg (8a2302ca 5c25 4d2d 9ffe 320080934aab 03)

FDA Label Image

Effexor Xr 75mg (8a2302ca 5c25 4d2d 9ffe 320080934aab 04)

Effexor Xr 75mg (8a2302ca 5c25 4d2d 9ffe 320080934aab 04)
Effexor XR 75mg extended-release capsules label, showing a package of 30 capsules. The label indicates each capsule contains venlafaxine and describes the capsule as peach-colored with 'W' and 'Effexor XR' on the cap and '75' on the body. The product is distributed by Physician Partner, Thousand Oaks, CA, and manufactured by Wyeth Pharmaceuticals Inc., Philadelphia, PA. The label includes NDC 21695-046-30 and emphasizes storage at controlled room temperature.*
FDA Label Image

Effexor Xr 150mg (8a2302ca 5c25 4d2d 9ffe 320080934aab 05)

Effexor Xr 150mg (8a2302ca 5c25 4d2d 9ffe 320080934aab 05)
Effexor XR 150mg ER Capsules label showing the product name, strength, and dosage form. The label indicates the capsules contain Venlafaxine HCl, have a dark orange cap and body with specific imprint details. Packaged by Physician Partner and manufactured by Wyeth Pharmaceuticals Inc. The label includes NDC 21695-047-15, lot number and expiration date placeholders, and storage instructions at 15°-30°C (59°-86°F).*

* 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.