Trazodone Hydrochloride
Product Images NDC 10544-534

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Trazodone Hydrochloride (NDC 10544-534). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Blenheim Pharmacal, 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

Trazodone Hydrochloride Tablets Usp 50 mg 100s Label (10544 534 30 50111 433 03)

Label for Trazodone Hydrochloride Tablets, USP 50 mg, containing 30 tablets. The label states Rx only and includes storage instructions to store at controlled room temperature (20-25°C/68-77°F) in a light-resistant container. The label shows the NDC 10544-534-30 and the manufacturer Blenheim Pharmacal, Inc., made in the USA.*

FDA Label Image

Structural Formula (Decd8580 3cdc 4a7c 9206 Da7eb496c988 01)

Chemical structure of Trazodone Hydrochloride showing its molecular arrangement with a triazolopyridine ring, piperazine ring, chlorophenyl group, and hydrochloride salt component.*

FDA Label Image

Image 1 (Decd8580 3cdc 4a7c 9206 Da7eb496c988 02)

Chemical structure diagram showing two triangular shapes each labeled with '50', representing the molecular formula or key structural features related to Trazodone Hydrochloride.*

FDA Label Image

Image 2 (Decd8580 3cdc 4a7c 9206 Da7eb496c988 03)

FDA Label Image

Image 3 (Decd8580 3cdc 4a7c 9206 Da7eb496c988 04)

Chemical structure of Trazodone Hydrochloride represented by two tetragonal shapes each containing the number 50, appearing to illustrate pill markings or dosage strength.*

FDA Label Image

Image 4 (Decd8580 3cdc 4a7c 9206 Da7eb496c988 05)

* 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.