Levothyroxine Sodium
Product Images NDC 70934-904

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Levothyroxine Sodium (NDC 70934-904). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Denton Pharma, Inc. Dba Northwind Pharmaceuticals, 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

Label (70934 904 30 Master Bottle Label Approval Rev A 09 21)

Label (70934 904 30 Master Bottle Label Approval   Rev A 09 21)
Label for Levothyroxine sodium Tablets, USP 75 mcg (0.075 mg) from Denton Pharma, Inc. DBA Northwind Pharmaceuticals. The label indicates a package of 30 tablets with NDC 70934-904-30, including dosage and storage instructions with emphasis on storage at 25°C and protection from light and moisture.*
FDA Label Image

Description (Levothyroxine Str)

Description (Levothyroxine Str)
Chemical structure diagram of Levothyroxine sodium showing the molecular arrangement, including iodine atoms, hydroxyl group, and carboxylate sodium salt with associated water molecules.*

* 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.