Structural Formula (Van0w 0000 01)
Vancomycin Hydrochloride Injection, Powder, Lyophilized, For Solution
Product Images NDC 25021-147
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Vancomycin Hydrochloride (NDC 25021-147). 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.
Package Label – Principal Display Panel – Vial Label (Van0w 0000 02)
Package Label – Principal Display Panel – Vial Label (Van0w 0000 03)
This is information related to a medication called Vancomycin Hydrochloride for Injection, USP. The text provides details such as the National Drug Code (NDC), the quantity per vial (1 gram), and instructions for intravenous use. It mentions that the medication must be reconstituted and further diluted as indicated in the package insert.*
Package Label – Principal Display Panel – Vial Label (Van0w 0000 04)
This is a description of a pharmaceutical product labeled as "Hydrochloride for Injection, USP" with a National Drug Code of 25021-148-30. The product is a sterile powder single-dose vial containing 1.5 grams of Vancomycin hydrochloride, which must be reconstituted with 30 mL of sterile water for intravenous use. The package insert contains important precautions, dosage information, and instructions for use. The product does not contain natural rubber latex in its container closure. The manufacturer is SAGENT Pharmaceuticals based in Schaumburg, IL, USA, and the product is made in India.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.
