Vancomycin Hydrochloride Injection, Powder, Lyophilized, For Solution
Product Images NDC 70436-021

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Vancomycin Hydrochloride (NDC 70436-021). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Slate Run Pharmaceuticals, 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.

FDA Label Image

Structural-formula (Image 01)

Chemical structure diagram of vancomycin hydrochloride showing molecular bonds, rings, and functional groups including hydroxyl (OH), amine (NH2), chlorine (Cl), and others consistent with the antibiotic's known complex glycopeptide structure.*

FDA Label Image

70436-020-82 (Image 02)

VANCOMYCIN HYDROCHLORIDE 500 mg per vial injection powder, lyophilized for intravenous use. The label indicates it is sterile, must be further diluted before use, and provides dosing and reconstitution instructions. Manufactured by Slate Run Pharmaceuticals, LLC.*

FDA Label Image

70436-021-82 (Image 03)

Label for Vancomycin Hydrochloride for Injection USP 1 g per vial, sterile lyophilized powder for intravenous use. The label emphasizes that the vial must be further diluted before use and includes storage instructions. Manufactured by Hainan Pedy Pharm Co., Ltd and distributed by Slate Run Pharmaceuticals, LLC.*

* 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.