Liothyronine Sodium Tablet
Product Images NDC 75907-039

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Liothyronine Sodium (NDC 75907-039). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dr. Reddy's Labratories 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 with multiple iodine atoms, a hydroxyl group, and a side chain containing an amino group and a sodium carboxylate group.*

FDA Label Image

Principle Display Panel-5mcg Tablet Bottle Label (Liothyronine 02)

Label for Liothyronine Sodium Tablets, USP 5 mcg, oral tablets, containing 100 tablets. The label includes storage instructions, dosage information, and distributor details for Dr. Reddy's Laboratories, Inc. Contact phone number and revision date are also visible.*

FDA Label Image

Principle Display Panel -25mg Tablet Bottle Label (Liothyronine 03)

Label for Liothyronine Sodium Tablets USP 25 mcg, 100 tablets, prescription oral tablets. The label includes storage instructions, dosage information, and is distributed by Dr. Reddy's Laboratories Inc., Princeton, NJ. The NDC number is partially visible.*

FDA Label Image

Principle Display Panel- 50mcg Tablet Bottle Label (Liothyronine 04)

Label for Liothyronine Sodium Tablets, USP 50 mcg, 100 tablets, by Dr. Reddy's Laboratories Inc. The label includes storage instructions (20° to 25°C), dispensing cautions, dosage references, and contact information. It features a barcode, NDC 75907-004-01, and the Dr. Reddy's logo.*

* 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.