Levothyroxine Sodium
Product Images NDC 70934-900

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 70934-900). 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 900 30 Master Bottle Label Approval Rev A 10 21)

Label (70934 900 30 Master Bottle Label Approval   Rev A 10 21)
This is a description of a medication called Levothyroxine in tablet form, with a strength of 50mcg (0.15mg). The National Drug Code (NDC) for this medication is given as 70934-900-30. The rest of the text appears to be unreadable or irrelevant.*
FDA Label Image

Description (Levothyroxine Str)

* 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.