Lorazepam Injection
Product Images NDC 65219-368

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Lorazepam (NDC 65219-368). 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

Loraz-img-01.jpg (Loraz Img 01)

Lorazepam 2 mg/mL injection label featuring an intravenous (IV) symbol. The label indicates the product is for IV use, consistent with the intramuscular and intravenous administration routes of Lorazepam injection by Fresenius Kabi USA, LLC.*

FDA Label Image

Loraz-img-02.jpg (Loraz Img 02)

FDA Label Image

Loraz-label-01.jpg (Loraz Label 01)

Label for Lorazepam Injection USP, 2 mg/mL, single-dose vial. The label states it is for intramuscular use and requires dilution for intravenous use. It includes storage instructions to protect from light and refrigerate. Manufactured by Fresenius Kabi USA, LLC, the label also shows NDC 65219-368-14 and a barcode.*

FDA Label Image

Loraz-label-02.jpg (Loraz Label 02)

Lorazepam Injection, USP 2 mg/mL vial label for intramuscular and intravenous use. The label specifies that dilution is required for intravenous use and that the product must be refrigerated. It includes a count of 25 single-dose 1 mL vials. Manufactured by Fresenius Kabi USA, LLC with NDC 65219-368-24.*

FDA Label Image

Loraz-struc-01.jpg (Loraz Struc 01)

Chemical structure diagram of lorazepam, showing its fused benzodiazepine ring system with two chlorine-substituted aromatic rings and characteristic functional groups.*

* 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.