Trazodone Hydrochloride Tablet
Product Images NDC 50111-561

10 FDA label images from Teva Pharmaceuticals Usa, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Trazodone Hydrochloride (NDC 50111-561). 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

Structural Formula (Image 1)

Structural Formula (Image 1)
Chemical structure of Trazodone Hydrochloride showing the molecular arrangement including a triazolopyridine ring, piperazine ring, chlorophenyl group, and associated hydrochloride component.*
FDA Label Image

150 mg 100s Rev. B 3/2016 (Image 10)

150 mg 100s Rev. B 3/2016 (Image 10)
Label for TraZODONE Hydrochloride Tablets USP 100 mg by Teva Pharmaceuticals USA, Inc. The label indicates the product contains 100 tablets per bottle. It includes dosing and storage instructions, a barcode, NDC 50111-434-01, and emphasizes pharmacist dispensing guidelines.*
FDA Label Image

50 mg (Image 2)

50 mg (Image 2)
Packaging label for Trazodone Hydrochloride tablets in 50 mg strength. The image shows two white tablets with a score line, each embossed with 'DB' on one side and '50' on the other, indicating the strength. The labeler is Teva Pharmaceuticals USA, Inc.*
FDA Label Image

75 mg (Image 3)

75 mg (Image 3)
The image shows a white tablet imprinted with "TEVA" on one side and "444" on the other side. This tablet corresponds to Trazodone Hydrochloride in tablet form, produced by Teva Pharmaceuticals USA, Inc.*
FDA Label Image

100 mg (Image 4)

100 mg (Image 4)
The image shows a white, round tablet split into two halves, each marked with the imprint 'G4' on one side, indicating a 50 mg strength of Trazodone Hydrochloride. The tablet is film-coated and scored for dividing. The labeler is Teva Pharmaceuticals USA, Inc.*
FDA Label Image

150 mg (Image 5)

150 mg (Image 5)
Packaging label for Trazodone Hydrochloride tablets by Teva Pharmaceuticals USA, Inc. The label displays the brand name "PLIVA" prominently in a bold, serif font at the top. It includes the dosage strength of 150 mg and the tablet form. The overall design is clean with a white and blue color scheme on a rectangular background.*
FDA Label Image

50mg (Image 6)

50mg (Image 6)
Label for Trazodone Hydrochloride Tablets, USP 50 mg, a tablet dosage form for further processing. The label indicates the quantity of 100 tablets and is manufactured by Teva Pharmaceuticals USA, Inc. It includes medication guide instructions and storage conditions. The NDC code is 50111-560-01.*
FDA Label Image

50 mg 100s (Image 7)

50 mg 100s (Image 7)
Label for Trazodone Hydrochloride Tablets USP 100 mg by Teva Pharmaceuticals USA, Inc. The label indicates 100 tablets with the instruction for pharmacists to dispense the accompanying Medication Guide to each patient. It includes storage instructions and a barcode on the left side.*
FDA Label Image

100mg (Image 8)

100mg (Image 8)
Label for Trazodone Hydrochloride Tablets USP 150 mg by Teva Pharmaceuticals USA, Inc. The label indicates a package of 100 tablets with an NDC code of 50111-450-01. It includes dispensing instructions and medication guide notes for pharmacists.*
FDA Label Image

100 mg 100s (Image 9)

100 mg 100s (Image 9)
Label for Trazodone Hydrochloride Tablets USP 50 mg by Teva Pharmaceuticals USA, Inc. The label indicates the product contains 100 tablets. It includes a barcode, NDC 50111-433-01, and advises pharmacists to dispense the accompanying medication guide to patients. The label also notes USP controlled room temperature storage and standard cautionary statements.*

* 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.