Vancomycin Hydrochloride Injection, Powder, Lyophilized, For Solution
Product Images NDC 63323-221

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Vancomycin Hydrochloride (NDC 63323-221). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fresenius Kabi, 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

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Chemical structure of Vancomycin Hydrochloride showing the detailed molecular arrangement including rings, hydroxyl groups, amine groups, chloride atoms, and hydrogen bonding within the molecule.*

FDA Label Image

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FDA Label Image

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Label of Vancomycin Hydrochloride injection, USP, 500 mg per vial. The label states it is for intravenous use only and must be further diluted before use. It is a prescription drug labeled by Fresenius Kabi USA, LLC, with the NDC number 63323-221-01.*

FDA Label Image

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Label for Vancomycin Hydrochloride injection powder, USP, for intravenous use. It specifies a strength of 500 mg per vial and notes that the product must be further diluted before use. The label includes a preservative warning and indicates the package contains 25 vials. The labeler is Fresenius Kabi USA, LLC.*

FDA Label Image

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Vancomycin Hydrochloride 750 mg per vial injection powder label for reconstitution. The label indicates intravenous use, specifies the strength of 750 mg per vial, and includes instructions to further dilute before use. The drug is labeled by Fresenius Kabi USA, LLC.*

FDA Label Image

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Vancomycin Hydrochloride 750 mg per vial injection powder lyophilized for solution label. The label shows the dosage strength as 750 mg per vial, for intravenous use, preservative-free formulation, and instructions that it must be further diluted before use. The labeler is Fresenius Kabi USA, LLC, and the package contains 10 vials.*

FDA Label Image

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Vancomycin Hydrochloride injection vial label showing a 1 gram per vial strength. The lyophilized powder for intravenous solution is indicated as preservative free. The label includes instructions to dilute before use and states it is for prescription use only. Labeler is Fresenius Kabi USA, LLC.*

FDA Label Image

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Vancomycin Hydrochloride injection label for intravenous use. The vial label shows a strength of 1 gram per vial in lyophilized powder form for solution. The label includes instructions that the product must be further diluted before use and states it contains 10 vials per package. The labeler is Fresenius Kabi USA, 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.