NDC Package 65628-272-10 Konvomep

Omeprazole And Sodium Bicarbonate Kit - View Billable Units, 11-Digit Format, RxNorm

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:
65628-272-10
Package Description:
1 KIT in 1 CARTON * 150 mL in 1 BOTTLE (65628-270-05) * 300 mL in 1 BOTTLE (65628-270-10) * 150 mL in 1 BOTTLE (65628-271-05) * 300 mL in 1 BOTTLE (65628-271-10) * 90 mL in 1 BOTTLE (65628-271-03) * 90 mL in 1 BOTTLE (65628-270-03)
Product Code:
Proprietary Name:
Konvomep
Non-Proprietary Name:
Omeprazole And Sodium Bicarbonate
Usage Information:
KONVOMEP is indicated in adults for: •short-term treatment (4 to 8 weeks) of active benign gastric ulcer.•reduction of risk of upper gastrointestinal (GI) bleeding in critically ill adult patients.
11-Digit NDC Billing Format:
65628027210
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 2625144 - omeprazole 2 MG/mL / sodium bicarbonate 84 MG/mL Oral Suspension
  • RxCUI: 2625144 - omeprazole 2 MG/ML / sodium bicarbonate 84 MG/ML Oral Suspension
  • RxCUI: 2625144 - omeprazole 2 MG/ML / NaHCO3 84 MG/ML Oral Suspension
  • RxCUI: 2625150 - KONVOMEP 2 MG / 84 MG in 1 mL Oral Suspension
  • RxCUI: 2625150 - omeprazole 2 MG/ML / sodium bicarbonate 84 MG/ML Oral Suspension [Konvomep]
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Azurity Pharmaceuticals, Inc.
    Dosage Form:
    Kit - A packaged collection of related material.
    Sample Package:
    No
    FDA Application Number:
    NDA213593
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    02-15-2023
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Code Structure:
    • 65628 - Azurity Pharmaceuticals, Inc.
      • 65628-272 - Konvomep
        • 65628-272-10 - 1 KIT in 1 CARTON * 150 mL in 1 BOTTLE (65628-270-05) * 300 mL in 1 BOTTLE (65628-270-10) * 150 mL in 1 BOTTLE (65628-271-05) * 300 mL in 1 BOTTLE (65628-271-10) * 90 mL in 1 BOTTLE (65628-271-03) * 90 mL in 1 BOTTLE (65628-270-03)

    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
    65628-272-031 KIT in 1 CARTON * 150 mL in 1 BOTTLE (65628-270-05) * 300 mL in 1 BOTTLE (65628-270-10) * 150 mL in 1 BOTTLE (65628-271-05) * 300 mL in 1 BOTTLE (65628-271-10) * 90 mL in 1 BOTTLE (65628-271-03) * 90 mL in 1 BOTTLE (65628-270-03)
    65628-272-051 KIT in 1 CARTON * 150 mL in 1 BOTTLE (65628-270-05) * 300 mL in 1 BOTTLE (65628-270-10) * 150 mL in 1 BOTTLE (65628-271-05) * 300 mL in 1 BOTTLE (65628-271-10) * 90 mL in 1 BOTTLE (65628-271-03) * 90 mL in 1 BOTTLE (65628-270-03)

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 65628-272-10?

    The NDC Packaged Code 65628-272-10 is assigned to a package of 1 kit in 1 carton * 150 ml in 1 bottle (65628-270-05) * 300 ml in 1 bottle (65628-270-10) * 150 ml in 1 bottle (65628-271-05) * 300 ml in 1 bottle (65628-271-10) * 90 ml in 1 bottle (65628-271-03) * 90 ml in 1 bottle (65628-270-03) of Konvomep, a human prescription drug labeled by Azurity Pharmaceuticals, Inc.. The product's dosage form is kit and is administered via form.

    Is NDC 65628-272 included in the NDC Directory?

    Yes, Konvomep with product code 65628-272 is active and included in the NDC Directory. The product was first marketed by Azurity Pharmaceuticals, Inc. on February 15, 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 NDC billing unit for package 65628-272-10?

    The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.

    What is the 11-digit format for NDC 65628-272-10?

    The 11-digit format is 65628027210. 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
    5-3-265628-272-105-4-265628-0272-10