Dactinomycin Injection, Powder, Lyophilized, For Solution
Product Images NDC 42658-008

3 FDA label images from Hisun Pharmaceuticals Usa, 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 Dactinomycin (NDC 42658-008). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hisun Pharmaceuticals Usa, 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

Chemical Structure (Hisun Dactinomycin 01)

Chemical Structure (Hisun Dactinomycin 01)
Chemical structure of dactinomycin showing its linear peptide chains with sarcosine, L-proline, and D-valine residues linked to a planar phenoxazine chromophore.*
FDA Label Image

Hisun-dactinomycin-02.jpg (Hisun Dactinomycin 02)

Hisun-dactinomycin-02.jpg (Hisun Dactinomycin 02)
Label for Dactinomycin for Injection, USP 500 mcg per vial, a cytotoxic agent in single-dose vial form. The vial is powder, lyophilized for intravenous solution preparation by reconstituting with 1.1 mL sterile water. Distributed by Hisun Pharmaceuticals USA, Inc., Bridgewater, NJ. Includes storage instructions and barcode.*
FDA Label Image

Hisun-dactinomycin-03.jpg (Hisun Dactinomycin 03)

Hisun-dactinomycin-03.jpg (Hisun Dactinomycin 03)
The packaging label for Dactinomycin for Injection, USP, 500 mcg per vial. The label highlights it as a single-dose vial containing lyophilized powder for intravenous use, distributed by Hisun Pharmaceuticals USA, Inc. The label includes storage instructions, a cytotoxic agent caution, and barcode. It indicates the product contains 500 mcg of dactinomycin with 20 mg mannitol as an inactive ingredient.*

* 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.