Vancomycin Hydrochloride Injection, Powder, Lyophilized, For Solution
Product Images NDC 25021-150

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 Vancomycin Hydrochloride (NDC 25021-150). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sagent Pharmaceuticals, 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

FDA Label Image

Structural Formula (Ste00 0005 01)

Structural Formula (Ste00 0005 01)
Chemical structure of vancomycin hydrochloride, illustrating the molecular arrangement typical to this antibiotic compound used in intravenous injection form.*
FDA Label Image

Package Label – Principal Display Panel – Vial Label (Ste00 0005 02)

Package Label – Principal Display Panel – Vial Label (Ste00 0005 02)
Label for Vancomycin Hydrochloride 500 mg per vial injection, powder, lyophilized, for intravenous use. The label indicates the product must be further diluted before use and provides dosing and storage instructions. It is manufactured for Sagent Pharmaceuticals, Schaumburg, IL, made in India.*
FDA Label Image

Package Label – Principal Display Panel – Vial Label (Ste00 0005 03)

Package Label – Principal Display Panel – Vial Label (Ste00 0005 03)
Label for Vancomycin Hydrochloride Injection, USP, 1 gram per vial, lyophilized powder for intravenous use. The label features the brand and generic name, dosage strength, route of administration, and a warning to dilute before use. Manufactured for Sagent Pharmaceuticals, Schaumburg, IL, made in India. Includes barcode, lot, expiration fields, and storage instructions.*

* 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.