Venxxiva Tablet, Delayed Release
Product Images NDC 70709-121

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Venxxiva (NDC 70709-121). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cycle Pharmaceuticals Ltd., 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
FDA Label Image

Image Description (Structuralformula)

Image Description (Structuralformula)
Chemical structure diagram of tiopronin showing its molecular formula with functional groups including a thiol (SH), amide (CONH), and carboxylic acid (COOH) group.*
FDA Label Image

Image Description (Tiopronintablets 100mg 300t)

Image Description (Tiopronintablets 100mg 300t)
Label for VENXXIVA 100 mg delayed-release tablets, containing tiopronin. The label states the package contains 300 tablets and includes usage warnings such as child-resistance and storage temperature. Manufactured for Torrent Pharmaceuticals Limited, India, and distributed by Cycle Pharmaceuticals Ltd, UK. The label also includes the NDC 70709-121-30 and a barcode.*
FDA Label Image

Image Description (Tiopronintablets 300mg 90t)

Image Description (Tiopronintablets 300mg 90t)
Label for VENXXIVA 300 mg delayed-release tablets containing tiopronin. The package contains 90 tablets and is marked Rx only. The label includes NDC 70709-123-90 and notes the product is manufactured by Torrent Pharmaceuticals Limited, India, and distributed by Cycle Pharmaceuticals Ltd, UK. Storage instructions and child-resistant package warning are also present.*

* 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.