Levothyroxine Sodium
Product Images NDC 53808-0446

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Levothyroxine Sodium (NDC 53808-0446). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by State Of Florida Doh Central Pharmacy, 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

Principal Display Panel (0.125 mg)

Principal Display Panel (0.125 mg)
Label for Levothyroxine 125 mcg tablets, quantity 30, packaged by DOH Central Pharmacy, Tallahassee, FL. The label includes lot number, expiration date, and a UPC barcode. It is marked RX Only and associated with the State of Florida DOH Central Pharmacy.*
FDA Label Image

Principal Display Panel (0.05 mg)

Principal Display Panel (0.05 mg)
Packaging label for Levothyroxine 50 mcg tablets, quantity 30, labeled by State of Florida DOH Central Pharmacy in Tallahassee, FL. The label includes lot number 186477A, expiration date 09/30/2010, and a barcode with UPC 305271342102.*
FDA Label Image

Principal Display Panel (0.075 mg)

Principal Display Panel (0.075 mg)
Label for Levothyroxine 75 mcg tablets, quantity 30. The label includes the lot number, expiration date (09/30/2010), and states the product is prescription only. It is packaged by the State of Florida DOH Central Pharmacy, Tallahassee, FL, and includes a UPC barcode.*
FDA Label Image

Chemical Structure (Levothyroxine 01)

Chemical Structure (Levothyroxine 01)
Chemical structure diagram of Levothyroxine Sodium showing its molecular composition with sodium and water components indicated.*

* 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.