Trazodone Hydrochloride Tablet
Product Images NDC 68071-4410

3 FDA label images from Nucare Pharmaceuticals,inc. · 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 Trazodone Hydrochloride (NDC 68071-4410). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nucare Pharmaceuticals,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 (288890b7 Bcd6 4e8e A437 Ac5cd56b27be 01)

Trazodone Hydrochloride Tablets Usp (288890b7 Bcd6 4e8e A437 Ac5cd56b27be 01)
Chemical structure of trazodone hydrochloride, showing its molecular framework including a chlorophenyl group, piperazine ring, and triazolopyridine core, with an associated hydrochloride molecule.*
FDA Label Image

Trazodone Hydrochloride Tablets Usp (288890b7 Bcd6 4e8e A437 Ac5cd56b27be 02)

Trazodone Hydrochloride Tablets Usp (288890b7 Bcd6 4e8e A437 Ac5cd56b27be 02)
Image shows a white, oval-shaped oral tablet of Trazodone Hydrochloride, scored and debossed with the imprint '6807' on one side. The tablet is identified as 50 mg strength, manufactured by NuCare Pharmaceuticals, Inc.*
FDA Label Image

68071 4410 03

68071 4410 03
Label for Trazodone Hydrochloride 50 mg tablets by NuCare Pharmaceuticals, Inc. The label shows the product strength (50 mg), quantity (#30 tablets), and dosage form (tablet). It includes manufacturer details, patient instructions placeholder, barcodes, and a warning to keep out of reach of children. Storage instructions specify controlled temperature (68-77°F).*

* 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.