Velsipity Tablet, Film Coated
Product Images NDC 0069-0274

View Photos of 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 Velsipity (NDC 0069-0274). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pfizer Laboratories Div Pfizer Inc, 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 (Velsipity 01)

Chemical Structure (Velsipity 01)
Chemical structure diagram of etrasimod, the active ingredient in Velsipity 2 mg film-coated tablets.*
FDA Label Image

Pfizer Logo (Velsipity 02)

FDA Label Image

Pfizer Logo (Velsipity 03)

FDA Label Image

Principal Display Panel (2 mg Tablet Bottle Label)

Principal Display Panel (2 mg Tablet Bottle Label)
Velsipity (etrasimod) 2 mg film-coated tablets label by Pfizer Laboratories Div Pfizer Inc. The label indicates the product contains 30 tablets for oral use. Storage instructions specify 20°C to 25°C (68°F to 77°F) with permitted excursions between 15°C to 30°C (59°F to 86°F). The label highlights the need to dispense with a Medication Guide and states the product is Rx only.*
FDA Label Image

Principal Display Panel (2 mg Tablet Bottle Carton)

Principal Display Panel (2 mg Tablet Bottle Carton)
Folded carton label for Velsipity (etrasimod) 2 mg film-coated tablets by Pfizer. The front panel shows the product name, active ingredient, strength, and tablet count (30 tablets). Other panels include storage instructions, dosing reference, and distribution information by Pfizer Labs, New York. Barcode and NDC 0069-0274 are also present.*

* 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.