Cibinqo Tablet, Film Coated
Product Images NDC 0069-0235

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Cibinqo (NDC 0069-0235). 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 (Cibinqo 01)

Chemical structure of abrocitinib, the active ingredient in Cibinqo. The molecular diagram depicts the arrangement of atoms and bonds characteristic to abrocitinib's chemical composition.*

FDA Label Image

Logo (Cibinqo 02)

FDA Label Image

Logo (Cibinqo 03)

FDA Label Image

Principal Display Panel (50 mg Tablet Bottle Label)

Cibinqo 50 mg tablets label by Pfizer Laboratories Division of Pfizer Inc. The film-coated oral tablet contains 50 mg abrocitinib. The label states storage instructions, dosing guidance, and indicates the package contains 30 tablets. It includes NDC 0069-0235-30 and barcode information, with origin noted as Made in Ireland.*

FDA Label Image

Principal Display Panel (100 mg Tablet Bottle Label)

Label for Cibinqo (abrocitinib) tablets 100 mg, a prescription oral film-coated tablet by Pfizer Laboratories Division of Pfizer Inc. The label states storage instructions, dosage information, and contains barcodes and NDC 0069-0335-30. The package contains 30 tablets and warnings include not to crush, split, or chew the tablets.*

FDA Label Image

Principal Display Panel (200 mg Tablet Bottle Label)

Cibinqo (abrocitinib) tablets 200 mg film-coated oral tablets label by Pfizer Laboratories Division of Pfizer Inc. Blue and white label showing 30 count, storage instructions between 20°C to 25°C, dosing information, and warnings not to crush, split, or chew tablets. Includes barcodes and National Drug Code (NDC) 0069-0435-30.*

* 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.