Carmustine Kit
Product Images NDC 71288-126

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Carmustine (NDC 71288-126). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Meitheal 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.

FDA Label Image

Figure (Car0x 0001 01)

Chemical structure of Carmustine showing its molecular formula with chlorine, nitrogen, carbon, oxygen, and hydrogen atoms arranged in specific bonds.*

FDA Label Image

Vial Label (Car0x 0001 10 V2)

Label for Carmustine for Injection, USP 100 mg per vial, a single-dose vial for intravenous infusion after reconstitution. The label instructs immediate refrigeration and disposal of unused portions. It includes storage and handling details, precautions, and is labeled for prescription use only. The label is from Meitheal Pharmaceuticals Inc.*

FDA Label Image

Diluent Label (Car0x 0001 11 V3)

Label for Dehydrated Alcohol Injection, USP sterile diluent for Carmustine for Injection, USP. The vial contains 3 mL and is intended for intravenous use. It is packaged with instructions to read the insert and stored refrigerated at 2-8°C (36-46°F). The label includes the NDC 71288-125-03 and the labeler Meitheal Pharmaceuticals Inc.*

FDA Label Image

Carton (Car0x 0001 12 V3)

Packaging label for Carmustine for Injection, USP 100 mg per vial, an intravenous infusion kit by Meitheal Pharmaceuticals Inc. The label includes storage instructions to refrigerate immediately, vial contents, dosing and handling precautions, and a barcode. The carton contains 1 vial of Carmustine 100 mg and 1 vial of sterile diluent for injection, USP 3 mL for reconstitution before use.*

* 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.