Thiotepa Injection, Powder, Lyophilized, For Solution
Product Images NDC 43598-171

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 Thiotepa (NDC 43598-171). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dr.reddy's Laboratories 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

Carton (Carton)

Carton (Carton)
Packaging label for Thiotepa for Injection, USP 100 mg/vial, a lyophilized powder for solution by Dr. Reddy's Laboratories Inc. The label states its use for intravenous, intracavitary, or intravesical administration. Storage instructions include refrigeration between 2°C to 8°C. The label also shows barcode areas, caution about cytotoxicity, and distributor information indicating it is made in India.*
FDA Label Image

Structure.jpg (Structure)

Structure.jpg (Structure)
Chemical structure of Thiotepa, showing a phosphorus atom double bonded to sulfur and bonded to three nitrogen atoms each connected to cycloalkyl groups.*
FDA Label Image

Vial (Vial)

Vial (Vial)
Label for Thiotepa injection USP 100 mg/vial by Dr. Reddy's Laboratories Inc. It indicates the product is for intravenous, intracavitary, or intravesical use, packaged as a single-dose vial with instructions to discard unused portions. The label includes a barcode, lot and expiration placeholders, and cautions the product as a cytotoxic agent. It also states the product is made in India and provides distributor details.*

* 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.