Lupkynis Capsule
Product Images NDC 75626-001

3 FDA label images from Aurinia Pharma U.s., Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Lupkynis (NDC 75626-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurinia Pharma U.s., 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

Lupkynis_carton (Lupkynis Carton 75)

Lupkynis_carton (Lupkynis Carton 75)
LUPKYNIS (voclosporin) 7.9 mg capsules carton label for oral use. The label states the product contains 180 capsules (3 wallets of 60 capsules each), each capsule with 7.9 mg voclosporin. Manufactured by Aurinia Pharmaceuticals Inc. and distributed by Aurinia Pharma U.S., Inc. The label includes storage instructions and pharmacist dispensing notes.*
FDA Label Image

Lupkynis_wallet (Lupkynis Wallet 65)

Lupkynis_wallet (Lupkynis Wallet 65)
Packaging label for LUPKYNIS 7.9 mg capsules containing voclosporin. The carton design includes manufacturer Aurinia Pharma U.S., Inc. The label shows the capsule dosage form and strength, usage route as oral, and includes detailed safety netting and blister pack illustrations outlining capsule placement and usage tips.*
FDA Label Image

Chemical_structure (Chemical Structure)

Chemical_structure (Chemical Structure)
Chemical structure diagram of Voclosporin, the active ingredient in LUPKYNIS 7.9 mg oral capsules by Aurinia Pharma U.S., Inc. The image shows the molecular arrangement with various atoms and bonds indicating the compound's complex cyclic structure.*

* 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.