Diprivan Injection, Emulsion
Product Images NDC 65219-800

5 FDA label images from Fresenius Kabi Usa, Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Diprivan (NDC 65219-800). 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

Dip0f 0001 01

Dip0f 0001 01
Chemical structure of propofol, showing the molecular arrangement including hydroxyl group and isopropyl substituents on a benzene ring. Molecular formula C12H18O and molecular weight 178.27 are indicated.*
FDA Label Image

Dip0f 0001 02

Dip0f 0001 02
A line graph showing plasma propofol concentration (mg/mL) over time (minutes) after the end of intravenous infusion. It depicts recovery profiles for three infusion durations: 1 hour, 10 hour, and 10 day, with concentration decreasing over time and a marked point labeled 'Awakening.'*
FDA Label Image

Dip0f 0001 03

FDA Label Image

Dip0f 0001 04

Dip0f 0001 04
Label for Diprivan (Propofol) injectable emulsion USP, 200 mg per 20 mL (10 mg per mL) for intravenous administration. The label indicates it is for single patient use only, with storage instructions between 4° to 25°C and a note to shake well before using. Manufactured for Fresenius Kabi USA, LLC, made in Sweden. The label also includes a barcode and warnings about using strict aseptic technique and discarding within 12 hours of opening.*
FDA Label Image

Dip0f 0001 05

Dip0f 0001 05
Packaging label for Diprivan (Propofol) injectable emulsion, USP, 200 mg per 20 mL (10 mg per mL) vials for intravenous administration. The label specifies ten 20 mL single-patient-use vials, with instructions to shake well before using. Manufactured by Fresenius Kabi USA, LLC, and indicates sterile, nonpyrogenic product with strict aseptic technique and EDTA antimicrobial preservative information.*

* 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.