Levothyroxine Sodium Tablet
Product Images NDC 71205-222

3 FDA label images from Proficient Rx Lp · 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 71205-222). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Proficient Rx Lp, 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

Chemical Structure (Levothyroxine Sodium Tablet Usp Jsp 1)

Chemical Structure (Levothyroxine Sodium Tablet Usp Jsp 1)
Chemical structure diagram of Levothyroxine Sodium, the active ingredient in the product. The diagram shows the molecular arrangement including phenolic rings, an ether linkage, and the sodium salt form with hydration indicated.*
FDA Label Image

71205-221-90 (Levothyroxine Sodium Tablet Usp Jsp 2)

71205-221-90 (Levothyroxine Sodium Tablet Usp Jsp 2)
Label for Levothyroxine Sodium 25mcg (0.025 mg) tablets, bottle of 90 tablets. The tablets are round, peach color coded, partial bisected, and debossed with JSP and ID Number 513. Manufactured by Jerome Stevens Pharmaceuticals, Inc., Bohemia, NY, and packaged by Proficient Rx LP, Thousand Oaks, CA. Storage instructions are 20°-25°C (68°-77°F).*
FDA Label Image

71205-222-90 (Levothyroxine Sodium Tablet Usp Jsp 7)

71205-222-90 (Levothyroxine Sodium Tablet Usp Jsp 7)
Label for Levothyroxine Sodium 112 mcg tablets, bottle of 90, manufactured by Jerome Stevens Pharmaceuticals and packaged by Proficient Rx LP. The label includes dosage strength, tablet description, NDC 71205-222-90, storage instructions, and serial/lot 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.