Mulpleta Tablet, Film Coated
Product Images NDC 84230-551

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 Mulpleta (NDC 84230-551). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Vancocin Italia Srl, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Trademark (Mulpleta 01)

Trademark (Mulpleta 01)
Mulpleta 3 mg film-coated tablets carton and bottle label for oral use. The product contains the active ingredient lusutrombopag. The labeler is VANCOCIN ITALIA SRL, and the package includes tablets with a strength of 3 mg each. The packaging shows both a white and yellow color scheme with printed product details and a safety seal on the bottle.*
FDA Label Image

Chemical Structure (Mulpleta 02)

Chemical Structure (Mulpleta 02)
Chemical structure of Lusutrombopag, the active ingredient in Mulpleta 3 mg film-coated tablets. The diagram shows the molecular arrangement of atoms including sulfur, chlorine, oxygen, and carbon within the compound.*
FDA Label Image

Principal Display Panel (3 mg Tablet Blister Card Carton)

Principal Display Panel (3 mg Tablet Blister Card Carton)
Mulpleta (lusutrombopag) 3 mg film-coated tablets packaging label for oral use. The label shows a box design with branding by Edding and manufacturer VANCOCIN ITALIA SRL. The box contains one blister card with 7 tablets and includes instructions for opening by pushing and holding a button. Storage instructions and dosage per tablet are also displayed.*

* 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.