NDC Package 0990-7715-02 Mannitol

Injection, Solution Intravenous - 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:
0990-7715-02
Package Description:
24 POUCH in 1 CASE / 1 BAG in 1 POUCH / 250 mL in 1 BAG (0990-7715-12)
Product Code:
Proprietary Name:
Mannitol
Non-Proprietary Name:
Mannitol
Substance Name:
Mannitol
Usage Information:
Mannitol Injection is indicated for the reduction of:intracranial pressure and treatment of cerebral edema;elevated intraocular pressure.
11-Digit NDC Billing Format:
00990771502
NDC to RxNorm Crosswalk:
  • RxCUI: 1791403 - mannitol 20 % in 250 ML Injection
  • RxCUI: 1791403 - 250 ML mannitol 200 MG/ML Injection
  • RxCUI: 1791403 - mannitol 20 % per 250 ML Injection
  • RxCUI: 1791408 - mannitol 20 % in 500 ML Injection
  • RxCUI: 1791408 - 500 ML mannitol 200 MG/ML Injection
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Icu Medical Inc.
    Dosage Form:
    Injection, Solution - A liquid preparation containing one or more drug substances dissolved in a suitable solvent or mixture of mutually miscible solvents that is suitable for injection.
    Administration Route(s):
  • Intravenous - Administration within or into a vein or veins.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    NDA019603
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    05-31-2019
    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
    0990-7715-0312 POUCH in 1 CASE / 1 BAG in 1 POUCH / 500 mL in 1 BAG (0990-7715-13)

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 0990-7715-02?

    The NDC Packaged Code 0990-7715-02 is assigned to a package of 24 pouch in 1 case / 1 bag in 1 pouch / 250 ml in 1 bag (0990-7715-12) of Mannitol, a human prescription drug labeled by Icu Medical Inc.. The product's dosage form is injection, solution and is administered via intravenous form.

    Is NDC 0990-7715 included in the NDC Directory?

    Yes, Mannitol with product code 0990-7715 is active and included in the NDC Directory. The product was first marketed by Icu Medical Inc. on May 31, 2019 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 0990-7715-02?

    The 11-digit format is 00990771502. 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 4-4-2 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
    4-4-20990-7715-025-4-200990-7715-02