Liothyronine Sodium Tablet
Product Images NDC 51407-384

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Liothyronine Sodium (NDC 51407-384). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Golden State Medical Supply, 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.

FDA Label Image

Chemical Structure (Liothyronine 01)

Chemical structure of Liothyronine Sodium showing two aromatic rings, iodine substituents, and a sodium carboxylate group connected through an ether linkage and a methane group to an amino acid moiety.*

FDA Label Image

Liothyronine Soidum Tabs (51407-384-01OL)

Liothyronine Sodium Tablets USP 5 mcg label showing a 100 tablets bottle package. The label includes the NDC number 51407-384-01 and the manufacturer GSMS Incorporated. It features dosage information, storage instructions, barcode, and safety warnings, emphasizing prescription-only status.*

FDA Label Image

Liothyronine Soidum Tabs (51407-385-01OL)

Label for Liothyronine Sodium Tablets USP, 25 mcg strength, in a bottle of 100 tablets. The label includes the NDC 51407-385-01, and instructions indicating prescription use (Rx Only). Marketed by GSMS Incorporated, Camarillo, CA. Storage and safety warnings are visible on the right side of the label.*

FDA Label Image

Liothyronine Soidum Tabs (51407-386-01OL)

Label for Liothyronine Sodium Tablets, USP 50 mcg, containing 100 tablets. The label displays the NDC 51407-386-01 and indicates the product is Rx Only. Manufactured or marketed by GSMS Incorporated. Additional text includes dosage form, lot, expiration, and storage instructions.*

* 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.