Propofol Injection, Emulsion
Product Images NDC 23155-345

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Propofol (NDC 23155-345). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Heritage Pharmaceuticals Inc. D/b/a Avet Pharmaceuticals Inc., 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

Figure A (A384f188 Bc32 4aac A2d6 9e31d20af881 01)

Chemical structure diagram of propofol, showing its molecular formula with a phenol ring and isopropyl groups attached.*

FDA Label Image

Figure B (A384f188 Bc32 4aac A2d6 9e31d20af881 02)

A line chart showing plasma propofol concentration (mg/mL) over time (minutes) after the end of infusion for different infusion durations: 10 days, 10 hours, and 1 hour. The graph includes a target plasma concentration line and indicates the awakening point during recovery.*

FDA Label Image

Avet Logo (A384f188 Bc32 4aac A2d6 9e31d20af881 03)

FDA Label Image

20 mL Carton (A384f188 Bc32 4aac A2d6 9e31d20af881 04)

Packaging label for Propofol Injectable Emulsion, USP 200 mg/20 mL (10 mg/mL) injection for intravenous use. The label specifies single patient use with 10 x 20 mL vials and includes directions to shake well before using. Manufactured by Emcure Pharmaceuticals Ltd. and labeled by Avet Pharmaceuticals Inc.*

FDA Label Image

20 mL Label (A384f188 Bc32 4aac A2d6 9e31d20af881 05)

Label for Propofol Injectable Emulsion, USP 200 mg/20 mL (10 mg/mL) intravenous injection emulsion by Avet Pharmaceuticals Inc. The label indicates it is for single patient use, with instructions to shake well before using, and includes storage and dosage information. The manufacturer is Emcure Pharmaceuticals Ltd., India.*

FDA Label Image

50 mL Carton Label (A384f188 Bc32 4aac A2d6 9e31d20af881 06)

The image shows a packaging label for Propofol Injectable Emulsion, USP 500 mg/50 mL (10 mg/mL) intravenous injection. The label specifies 20 x 50 mL vials for single patient use, with instructions to shake well before using. Manufactured by Emcure Pharmaceuticals Ltd. and Avet Pharmaceuticals Inc., the label includes storage instructions (store between 4° to 25°C) and warnings about aseptic technique and antimicrobial content.*

FDA Label Image

50 mL Label (A384f188 Bc32 4aac A2d6 9e31d20af881 07)

Label for Propofol Injectable Emulsion, USP 10 mg/mL in a 50 mL vial (500 mg total), for intravenous use. The label states 'Shake well before using' and 'Single Patient Use Only.' It includes storage instructions, manufacturing details by Emcure Pharmaceuticals Ltd., and labeling by Avet Pharmaceuticals Inc., with barcode and lot information visible.*

FDA Label Image

100 mL Carton Label (A384f188 Bc32 4aac A2d6 9e31d20af881 08)

Label for Propofol Injectable Emulsion USP 1,000 mg/100 mL (10 mg/mL) intravenous injection in 10 x 100 mL vials for single patient use. The product is manufactured by Emcure Pharmaceuticals Ltd. and labeled for Avet Pharmaceuticals Inc. The label instructs to shake well before using and states it is for intravenous administration only. Packaging includes barcodes and storage instructions.*

FDA Label Image

100 mL Label (A384f188 Bc32 4aac A2d6 9e31d20af881 09)

Label for propofol injection emulsion USP, 10 mg/mL (1,000 mg/100 mL) for intravenous administration. The label instructs to shake well before using and notes it is a 100 mL vial for single patient use only. It includes storage and handling instructions, active component details, and manufacturer information for Emcure Pharmaceuticals Ltd. and Avet Pharmaceuticals Inc.*

* 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.