1. Home
  2. Labeler Index
  3. Genixus
  4. 80700-113
  5. NDC Package Code: 80700-113-11 Propofol 1%

NDC Package 80700-113-11 Propofol 1%

Injection, Emulsion Intravenous - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
80700-113-11
Package Description:
10 SYRINGE, PLASTIC in 1 BAG / 10 mL in 1 SYRINGE, PLASTIC (80700-113-10)
Product Code:
80700-113
Proprietary Name:
Propofol 1%
Non-Proprietary Name:
Propofol 1%
Substance Name:
Propofol
11-Digit NDC Billing Format:
80700011311
NDC to RxNorm Crosswalk:
  • RxCUI: 312674 - propofol 10 MG/ML Injectable Suspension
  • RxCUI: 312674 - propofol 1 % Injectable Suspension
  • RxCUI: 312674 - propofol 200 MG per 20 ML Injectable Suspension
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Genixus
    Dosage Form:
    Injection, Emulsion - An emulsion consisting of a sterile, pyrogen-free preparation intended to be administered parenterally.
    Administration Route(s):
  • Intravenous - Administration within or into a vein or veins.
    • Active Ingredient(s):
  • PROPOFOL 10 mg/mL
    • Pharmacologic Class(es):
  • General Anesthesia - [PE] (Physiologic Effect)
  • General Anesthetic - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
    Start Marketing Date:
    03-29-2023
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Code Structure:

    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 disclaimer below.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    80700-113-1225 SYRINGE, PLASTIC in 1 BAG / 10 mL in 1 SYRINGE, PLASTIC (80700-113-10)
    80700-113-2110 SYRINGE, PLASTIC in 1 BAG / 20 mL in 1 SYRINGE, PLASTIC (80700-113-20)
    80700-113-2225 SYRINGE, PLASTIC in 1 BAG / 20 mL in 1 SYRINGE, PLASTIC (80700-113-20)

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 80700-113-11?

    The NDC Packaged Code 80700-113-11 is assigned to a package of 10 syringe, plastic in 1 bag / 10 ml in 1 syringe, plastic (80700-113-10) of Propofol 1%, a human prescription drug labeled by Genixus. The product's dosage form is injection, emulsion and is administered via intravenous form.

    Is NDC 80700-113 included in the NDC Directory?

    Yes, Propofol 1% with product code 80700-113 is active and included in the NDC Directory. The product was first marketed by Genixus on March 29, 2023 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 80700-113-11?

    The 11-digit format is 80700011311. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-280700-113-115-4-280700-0113-11