Liothyronine Sodium Tablet
Product Images NDC 0093-2178

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Liothyronine Sodium (NDC 0093-2178). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Teva Pharmaceuticals Usa, 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

Structure (1 1)

Chemical structure of Liothyronine Sodium, showing the molecular arrangement including iodine atoms, hydroxyl group, and sodium carboxylate group, consistent with the thyroid hormone analog used in oral tablets by Teva Pharmaceuticals USA, Inc.*

FDA Label Image

5 Mcg 100s (1 2)

Liothyronine Sodium Tablets USP 5 mcg oral tablets label by Teva Pharmaceuticals USA, Inc. The label shows the NDC 0093-2179-01 and indicates the package contains 100 tablets. Storage instructions specify 20 to 25°C (68° to 77°F) with a child-resistant closure required. The label includes dosing equivalency information and advises use under physician supervision.*

FDA Label Image

25 Mcg 100s (1 3)

Label for Liothyronine Sodium Tablets USP 25 mcg by Teva Pharmaceuticals USA, Inc. The label indicates an oral tablet prescription drug, with a package size of 100 tablets. Storage instructions, usual dosage guidance, and sodium content per tablet are included along with the NDC 0093-2178-01.*

FDA Label Image

50 Mcg 100 (1 4)

Label for Liothyronine Sodium Tablets USP 50 mcg by Teva Pharmaceuticals USA, Inc. The label specifies 100 tablets per package, prescription use only, and includes storage instructions, lot, and expiration placeholders.*

* 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.