Propofol Injection, Emulsion
NDC Package 71288-730-51

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. NDC HCPCS Crosswalk
    3. Frequently Asked Questions

Package Information

Propofol injection is propofol Injectable Emulsion is an intravenous general anesthetic and sedation drug indicated for:Induction of General Anesthesia for Patients Greater than or Equal to 3 Years of AgeMaintenance of General Anesthesia for Patients Greater than or Equal to 2 Months of AgeInitiation and Maintenance of Monitored Anesthesia Care (MAC) Sedation in Adult PatientsSedation for Adult Patients in Combination with Regional AnesthesiaIntensive Care Unit (ICU) Sedation of Intubated, Mechanically Ventilated Adult PatientsLimitations of UsePropofol Injectable Emulsion is not recommended for induction of anesthesia below the age of 3 years or for maintenance of anesthesia below the age of 2 months because its safety and effectiveness have not been established in those populations [see Pediatric Use (8.4)].Safety, effectiveness and dosing guidelines for Propofol Injectable Emulsion have not been established for MAC sedation in the pediatric population; therefore, it is not recommended for this use [see Pediatric Use (8.4)].Propofol Injectable Emulsion is not indicated for use in Pediatric ICU sedation since the safety of this regimen has not been established [see Pediatric Use (8.4)]. This formulation utilizes a injection, emulsion delivery system. Marketed by Meitheal Pharmaceuticals Inc., this product is identified by NDC 71288-730 and is authorized under FDA application ANDA217945.

Identification & Billing

NDC Package Code
71288-730-51
Package Description
10 VIAL in 1 CARTON / 50 mL in 1 VIAL (71288-730-50)
Product Code
71288-730
11-Digit Billing Format
71288073051
Billing Unit
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Propofol
Non-Proprietary Name
Propofol
Substance Name
Propofol
Dosage Form
Injection, Emulsion - An emulsion consisting of a sterile, pyrogen-free preparation intended to be administered parenterally.
Administration Route
Intravenous - Administration within or into a vein or veins.
Active Ingredient(s)
PROPOFOL 10 mg/mL
Pharmacologic Class
Usage Information
Propofol Injectable Emulsion is an intravenous general anesthetic and sedation drug indicated for:Induction of General Anesthesia for Patients Greater than or Equal to 3 Years of AgeMaintenance of General Anesthesia for Patients Greater than or Equal to 2 Months of AgeInitiation and Maintenance of Monitored Anesthesia Care (MAC) Sedation in Adult PatientsSedation for Adult Patients in Combination with Regional AnesthesiaIntensive Care Unit (ICU) Sedation of Intubated, Mechanically Ventilated Adult PatientsLimitations of UsePropofol Injectable Emulsion is not recommended for induction of anesthesia below the age of 3 years or for maintenance of anesthesia below the age of 2 months because its safety and effectiveness have not been established in those populations [see Pediatric Use (8.4)].Safety, effectiveness and dosing guidelines for Propofol Injectable Emulsion have not been established for MAC sedation in the pediatric population; therefore, it is not recommended for this use [see Pediatric Use (8.4)].Propofol Injectable Emulsion is not indicated for use in Pediatric ICU sedation since the safety of this regimen has not been established [see Pediatric Use (8.4)].

Regulatory & Marketing

Labeler Name
Meitheal Pharmaceuticals Inc.
Product Type
Human Prescription Drug
FDA Application #
ANDA217945
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
12-02-2025
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the full disclaimer at the bottom of this page.

Billing & HCPCS Mapping

To facilitate insurance claims and reimbursement, this drug package is mapped to specific HCPCS administrative codes. This crosswalk aligns clinical data with the billing standards used in ASP (Average Sales Price), AWP, and OPPS payment systems. Use the cards below to identify the correct billable units for provider claims.

J2704
Source: PDAC
INJECTION, PROPOFOL, 10 MG
HCPCS Dosage 10 MG
Units / Pkg

Note for Medical Coders: These mappings are synthesized from various CMS datasets including OPPS, PrEP, and DAC (Data Analysis and Coding) contractors. Always confirm unit conversions against the current quarter's pricing files before final submission.

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 71288-730-51 identifies a specific commercial package of 10 vial in 1 carton / 50 ml in 1 vial (71288-730-50) of Propofol, a human prescription drug labeled by Meitheal Pharmaceuticals Inc.. This injection, emulsion is formulated for intravenous use and contains propofol as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Meitheal Pharmaceuticals Inc. on December 02, 2025. The current certification is valid through December 31, 2026.

How is this Meitheal Pharmaceuticals Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 71288073051. Quantities are measured in per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
71288-730-51
11-Digit CMS (5-4-2)
71288-0730-51

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.