Chemical Structure (Image 01)
Chemical structure of Vancomycin Hydrochloride as depicted in the image, showing detailed molecular bonds and configuration.*
Vancomycin Hydrochloride Injection, Powder, Lyophilized, For Solution
Product Images NDC 67457-705
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Vancomycin Hydrochloride (NDC 67457-705). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Mylan Institutional Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Product Images & Figures Index
250 mg Carton (Image 02)
Packaging label for Vancomycin Hydrochloride 250 mg/vial sterile powder for injection, USP, indicated for intravenous use. The label indicates 10 single-dose vials per package. Manufactured by Mylan Institutional LLC, the label includes storage and preparation instructions, a barcode, and the NDC 67457-822-99.*
750 mg Carton (Image 03)
Packaging label for Vancomycin Hydrochloride for Injection, USP, 750 mg per vial sterile powder. The label indicates it is for intravenous use and must be further diluted after reconstitution. The product is supplied as 10 single-dose vials of 750 mg each and is manufactured by Mylan Institutional LLC.*
1.5 G Carton (Image 04)
Packaging label for Vancomycin Hydrochloride for Injection, USP, 1.5 g/vial sterile powder for intravenous use. The label is for 10 single-dose vials of 1.5 g each, manufactured by Mylan Institutional LLC. The label includes instructions that the product must be further diluted after reconstitution and storage information.*
1.25 G Carton (Image 05)
Packaging label for Vancomycin Hydrochloride Injection USP 1.25 g per vial sterile powder by Mylan Institutional LLC. The label indicates a package containing 10 single-dose vials of 1.25 g strength each. It includes instructions noting the product is for intravenous use, to be reconstituted and further diluted before use, and storage information. The label displays the NDC 67457-823-99 and company branding.*
* 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.
