Figure A (B337fdd5 9e14 4d4b 88ff D9e6d6b16e19 01)
Propofol Injection, Emulsion
Product Images NDC 16714-690
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Product Visual Gallery
This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Propofol (NDC 16714-690). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Northstar Rx 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.
Product Images & Figures Index
Figure B (B337fdd5 9e14 4d4b 88ff D9e6d6b16e19 02)
20 mL Carton (B337fdd5 9e14 4d4b 88ff D9e6d6b16e19 03)
Propofol Injectable Emulsion, USP is a medication used for intravenous administration, with each vial containing 200 mg/20mL at a concentration of 10mg/mL. It contains Soybean oil, USP, glycerol, USP, egg lecithin, NF, and disodium edetate anhydrous, USP, with sodium hydroxide, NF to adjust pH. The medication should only be administered by trained persons in general anesthesia and must not be involved in the surgery. Patients should be continuously monitored for the maintenance of their airways, artificial ventilation, and oxygen enrichment, with facilities available for circulatory resuscitation in case of emergency. It is sterile and non-pyrogenic and must be stored between 4 to 25°C (40°to T7°F). It is manufactured by Emcure Pharmaceuticals Ltd, India, and comes with batch details and 2D barcoding for easy traceability.*
20 mL Label (B337fdd5 9e14 4d4b 88ff D9e6d6b16e19 04)
Propofol Injectable Emulsion, USP is a sterile and nonpyrogenic solution for intravenous administration. Each vial contains 200mg/20 mL of 10 mg/mL propofol. The solution should be strictly used under aseptic technique and discarded after 12 hours of opening. It is composed of propofol, soybean oil, glycerol, egg lecithin, disodium edetate anhydrous, and sodium hydroxide for pH adjustment. The medication is manufactured by Emcure Pharmaceuticals Ltd. in India and is labeled for use by Northstar Rx LLC in Memphis, TN. Please refer to the package insert for dosage and storage instructions.*
50 mL Carton Label (B337fdd5 9e14 4d4b 88ff D9e6d6b16e19 05)
Propofol Injectable Emulsion, USP is a medication manufactured by Emcure Pharmaceuticals Ltd. in India and distributed in the US by Northstar Rx LLC. It is used for intravenous administration during surgical or diagnostic procedures and should only be administered by trained personnel. The formulation contains soybean oil, glycerol, egg lecithin, and disodium edetate anhydrous. It is stored between 4° to 25°C and should not be frozen. The vials should be discarded after 12 hours of opening due to the presence of EDTA, which inhibits microbial growth. The package insert should be consulted for dosage information.*
50 mL Label (B337fdd5 9e14 4d4b 88ff D9e6d6b16e19 06)
Propofol Injectable is a sterile, nonpyrogenic emulsion recommended for intravenous administration. The formulation consists of propofol, soybean oil, glycerol, lecithin, disodium edetate, and sodium hydroxide. It is manufactured by Emcure Pharmaceuticals Ltd in Sanand, Ahmedabad and is for single patient use only. The package insert should be consulted for dosage information. The product should be stored at a temperature range of 4° to 25°C and should not be frozen. The product includes EDTA, which inhibits microbial growth for up to 12 hours; therefore, it should be discarded within 12 hours of opening. Strict aseptic technique should be followed during use.*
100 mL Carton Label (B337fdd5 9e14 4d4b 88ff D9e6d6b16e19 07)
Propofol Injectable Emulsion, USP is a medication used for intravenous administration in general anesthesia. It includes 1000mg of propofol per 100mL, soybean oil, glycerol, egg lecithin, and disodium edetate anhydrous. The medication should be used only by persons trained in the administration of general anesthesia, and it is necessary to have all the required devices for airway, ventilation, and oxygen enrichment, and circulatory resuscitation nearby. The medication cannot be stored below 4°C or above 25°C, and it contains EDTA, which inhibits microbial growth for up to 12 hours. The package includes 10x100mL vials for single patient use only.*
100 mL Label (B337fdd5 9e14 4d4b 88ff D9e6d6b16e19 08)
Propofol Injectable Emulsion, USP is a sterile, non-pyrogenic solution administered intravenously. The formulation contains propofol as an active ingredient, along with soybean oil, glycerol, egg lecithin, and disodium edetate anhydrous. The solution is supplied in a 100 mL vial for single-patient use only. Before using, shake the vial well and use strict aseptic technique. It is recommended to discard the solution within 12 hours of opening as it contains EDTA that inhibits microbial growth up to 12 hours. Dosage instructions should be followed as given in the package insert. The solution should be stored between 4 to 25°C, and not frozen. However, due to poor quality , some parts of the text might be distorted or missing.*
* 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.
