Lynkuet Capsule
Product Images NDC 50419-475

View Photos of 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 Lynkuet (NDC 50419-475). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bayer Healthcare Pharmaceuticals 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 (Lynkuet 01)

Chemical Structure (Lynkuet 01)
Chemical structure of elinzanetant, the active ingredient in LYNKUET capsules. The structure shows the arrangement of atoms and bonds including oxygen, nitrogen, fluorine, and trifluoromethyl groups characteristic of the molecule.*
FDA Label Image

Principal Display Panel (60 mg Capsule Blister Pack)

Principal Display Panel (60 mg Capsule Blister Pack)
LYNKUET 60 mg capsules packaging label showing six individual capsule compartments. Each label includes the product name Lynkuet, generic name elinzanetant, strength of 60 mg per capsule, a barcode, NDC 50419-475-01, and Pfizer HealthCare Pharmaceuticals Inc. as the labeler. The label also states Rx only and has spaces for lot and expiration dates.*
FDA Label Image

Principal Display Panel (60 mg Capsule Blister Pack Carton)

Principal Display Panel (60 mg Capsule Blister Pack Carton)
LYNKUET 60 mg capsules packaging label displaying the product name and active ingredient elinzanetant. The label states it contains 60 capsules in 5 blister cards of 12 capsules each. The label includes Bayer logos and notes that the product is distributed by Bayer HealthCare Pharmaceuticals Inc. in Whippany, NJ, and manufactured in Germany. Storage instructions and a contact number are also visible.*

* 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.