Propofol Injection, Emulsion
Product Images NDC 83854-018

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Propofol (NDC 83854-018). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Anthea Pharma Private Limited, 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

"image Description" (Figure 1)

A line chart showing plasma propofol concentration (mg/mL) over time (minutes) after the end of infusion. It illustrates the recovery profiles following 1-hour, 10-hour, and 10-day infusions, with a reference line indicating the awakening concentration.*

FDA Label Image

"image Description" (Propofol 200mg 20ml Cart Labl)

Packaging label for Propofol Injectable Emulsion, USP, 10 mg/mL (200 mg/20 mL) intravenous injection emulsion. The label indicates a carton containing 10 single-dose 20 mL vials. The product is manufactured by Anthea Pharma Private Limited and carries the NDC 83854-018-10. Instructions to shake well before use are prominently displayed.*

FDA Label Image

"image Description" (Propofol 200mg 20ml Cont Labl)

Label for Propofol Injectable Emulsion USP 200 mg/20 mL (10 mg/mL) single-dose vial. It is for intravenous administration and requires shaking before use. Manufactured by Anthea Pharma Private Limited in Hyderabad, India. The label includes storage instructions, a warning about EDTA content inhibiting microbial growth up to 12 hours, and notes to use strict aseptic technique.*

FDA Label Image

"image Description" (Structure 1)

Chemical structure diagram of propofol showing the aromatic ring with hydroxyl and isopropyl groups attached, consistent with its molecular formula.*

* 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.