Tiopronin Tablet, Delayed Release
Product Images NDC 0480-9227

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 Tiopronin (NDC 0480-9227). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Teva 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.

Product Images & Figures Index

FDA Label Image

New (Image 1)

New (Image 1)
Chemical structure diagram of Tiopronin, showing its molecular arrangement including a thiol (SH) group and carboxylic acid group. This structural formula represents the active ingredient Tiopronin used in tablet form by Teva Pharmaceuticals.*
FDA Label Image

Launch (Image 2)

Launch (Image 2)
Label for Tiopronin Delayed-Release Tablets, 100 mg strength, oral dosage form. The label indicates a package size of 300 tablets and is manufactured for Teva Pharmaceuticals, Inc. The label includes storage information, dosage guidance referring to prescribing information, and manufacturing details specifying production in India by Watson Pharma Private Limited. A barcode and serialization coding area are also present.*
FDA Label Image

Launch (Image 3)

Launch (Image 3)
Tiopronin Delayed-Release Tablets 300 mg label from Teva Pharmaceuticals, Inc. The label indicates a package size of 90 tablets and notes each delayed-release tablet contains 300 mg of tiopronin. Additional information includes storage instructions, manufacturer details, and an NDC barcode.*

* 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.