Thiotepa Injection, Powder, Lyophilized, For Solution
Product Images NDC 43598-650

3 FDA label images from Dr.reddy's Laboratories 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 Thiotepa (NDC 43598-650). 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 Injection USP 15 mg/vial from Dr.Reddy's Laboratories Inc. The label details this is a single-dose vial for intravenous, intracavitary, or intravesical use. It advises storage between 2° to 8°C, protection from light, and includes handling cautions for this sterile, non-pyrogenic injectable powder for solution. The label displays NDC 43598-650-11 with barcodes and distributor information.*
FDA Label Image

Structure (Structure)

Structure (Structure)
Chemical structure of Thiotepa showing a phosphorus atom bonded to three nitrogen atoms forming a ring with ethylene groups and a sulfur atom.*
FDA Label Image

Vial (Vial)

Vial (Vial)
Thiotepa For Injection, USP 15 mg/vial, lyophilized powder for solution injection. The label indicates use for intravenous, intracavitary, or intravesical administration. Labeled as single-dose vial by Dr. Reddy's Laboratories Inc., made in India, with storage instructions for refrigeration between 2° to 8°C. Includes a barcode and spaces for lot and expiration date.*

* 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.