Oxacillin Injection, Powder, For Solution
Product Images NDC 63323-811

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Oxacillin (NDC 63323-811). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fresenius Kabi Usa, 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

Structure (Oxa0o 0000 01)

Chemical structure of Oxacillin Sodium, shown as a detailed molecular diagram including the beta-lactam ring, thiazolidine ring, and side chains characteristic of the antibiotic structure, with indication of a water molecule (H2O) associated.*

FDA Label Image

Logo (Oxa0o 0000 02)

FDA Label Image

Vialpbp (Oxa0o 0000 03)

Oxacillin for Injection, USP 10 grams per Pharmacy Bulk Package powder label for intravenous use. The label states the product is sterile, nonpyrogenic, and preservative-free. It is manufactured by Fresenius Kabi USA, LLC, Lake Zurich, IL, and made in Italy. The label includes reconstitution instructions, storage conditions, and warnings that it is for pharmacy bulk use, not direct infusion.*

FDA Label Image

Pbpctn (Oxa0o 0000 04)

Label for Oxacillin for Injection, USP 10 grams per Pharmacy Bulk Package by Fresenius Kabi USA, LLC. This is a pharmacy bulk package bottle containing Oxacillin sodium powder for injection prepared for intravenous use. The label includes reconstitution instructions, storage conditions, product inquiry contact, and notes that the container is sterile, nonpyrogenic, and preservative-free. It also emphasizes the package is not for direct infusion and should be used only to prepare intravenous admixtures.*

* 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.