Mulpleta Tablet, Film Coated
Product Images NDC 59630-551

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Mulpleta (NDC 59630-551). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Shionogi 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

Trademark (Mulpleta 01)

Mulpleta 3 mg film-coated tablets carton and blister pack for oral use. The packaging includes the brand name Mulpleta, strength 3 mg, dosage form of film-coated tablets, and the labeler SHIONOGI INC. The blister pack inside the carton contains multiple tablets.*

FDA Label Image

Chemical Structure (Mulpleta 02)

Chemical structure of Lusutrombopag, the active ingredient in Mulpleta 3 mg oral film-coated tablets by Shionogi Inc. The structure shows the molecular arrangement of atoms including sulfur, oxygen, chlorine, and a carboxylic acid group as part of the compound.*

FDA Label Image

Principal Display Panel (3 mg Tablet Blister Card Carton)

Mulpleta 3 mg film-coated tablets packaging label for oral use by Shionogi Inc. The carton contains 7 tablets of lusutrombopag, with instructions for storage between 20°C to 25°C and opening directions featuring a push and pull mechanism. The label notes prescription-only status and includes a barcode and manufacturer details.*

FDA Label Image

Mulpleta 04

Packaging label for Mulpleta (lusutrombopag) tablets, 3 mg oral film-coated tablets by Shionogi Inc. The label indicates a prescription drug intended for oral use, supplied as one blister card containing 7 tablets. Instructions for use and storage conditions (20°C to 25°C) are also provided, along with a barcode and manufacturer information.*

* 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.