Levothyroxine Sodium
Product Images NDC 52959-920

View Photos of 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 52959-920). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by H.j. Harkins Company, 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 (Levothyroxine 01)

Chemical Structure (Levothyroxine 01)
Chemical structure of Levothyroxine Sodium showing the molecular arrangement including phenol groups, an ether linkage, and the sodium salt form with associated water molecules.*
FDA Label Image

Principal Display Panel (0.1 mg)

Principal Display Panel (0.1 mg)
Levothyroxine Sodium 100 mcg tablet label by H.J. Harkins Company, Inc. The label shows the product name, strength, dosage form, lot number LEV105LH, manufacturer Lannett, expiration date 01/11, and comparison to Synthroid with NDC 0527-1345-01. It includes quantity 100 tablets per bottle, location PA, and usage instructions to take as directed by a doctor. Several smaller label copies are shown on the right side.*
FDA Label Image

Principal Display Panel (0.125 mg)

Principal Display Panel (0.125 mg)
Packaging label for Levothyroxine Sodium 125 mcg tablets by H.J. Harkins Company, Inc., manufactured by Lannett in Philadelphia, PA. The label includes lot number LVN05LH, expiration date 06/11, and references comparison to Synthroid (NDC 0527-1347-01). Tablets are described as brown, tan, round, with a pill ID. The label states a quantity of 100 tablets per package.*

* 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.