Levothyroxine Sodium Injection, Powder, Lyophilized, For Solution
Product Images NDC 72266-261

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 Levothyroxine Sodium (NDC 72266-261). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fosun Pharma Usa 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.

Product Images & Figures Index

FDA Label Image

Carton (Carton)

Carton (Carton)
Packaging label for Levothyroxine Sodium Injection 100 mcg per vial, lyophilized powder for intravenous use. The label indicates a single-dose vial with preservative-free contents, distributed by Fosun Pharma USA Inc. The label includes NDC 72266-261-01 and storage instructions, and states the product is made in India.*
FDA Label Image

Container (Container)

Container (Container)
Label for Levothyroxine Sodium injection, 100 mcg per vial, lyophilized powder for intravenous use. The single-dose vial label notes preservative-free content, storage instructions, directions for reconstitution with 5 mL sodium chloride injection, and discard instructions for unused portions. Distributed by Fosun Pharma USA Inc.*
FDA Label Image

Structure (Structure)

Structure (Structure)
Chemical structure diagram of Levothyroxine Sodium Anhydrous, depicting its molecular arrangement including iodine atoms and amino acid components, corresponding to the active ingredient in Levothyroxine Sodium injection powder by Fosun Pharma USA Inc.*

* 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.