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  5. NDC Package Code: 0338-9647-12 Vasopressin In 0.9% Sodium Chloride

NDC Package 0338-9647-12 Vasopressin In 0.9% Sodium Chloride

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

Table of Contents

    1. Package Information
    2. 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:
0338-9647-12
Package Description:
12 BAG in 1 CARTON / 100 mL in 1 BAG
Product Code:
0338-9647
Proprietary Name:
Vasopressin In 0.9% Sodium Chloride
Non-Proprietary Name:
Vasopressin In 0.9% Sodium Chloride
Substance Name:
Vasopressin
Usage Information:
Vasopressin in Sodium Chloride Injection is indicated to increase blood pressure in adults with vasodilatory shock who remain hypotensive despite fluids and catecholamines.
11-Digit NDC Billing Format:
00338964712
NDC to RxNorm Crosswalk:
  • RxCUI: 2399907 - vasopressin (USP) 40 UNT in 100 ML Injection
  • RxCUI: 2399907 - 100 ML vasopressin (USP) 0.4 UNT/ML Injection
  • RxCUI: 2399907 - vasopressin (USP) 40 UNT per 100 ML Injection
  • RxCUI: 2591428 - vasopressin (USP) 20 UNT in 100 ML Injection
  • RxCUI: 2591428 - 100 ML vasopressin (USP) 0.2 UNT/ML Injection
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Baxter Healthcare Corporation
    Dosage Form:
    Injection - A sterile preparation intended for parenteral use; five distinct classes of injections exist as defined by the USP.
    Administration Route(s):
  • Intravenous - Administration within or into a vein or veins.
    • Active Ingredient(s):
  • VASOPRESSIN 40 [USP'U]/100mL
    • Pharmacologic Class(es):
  • Decreased Diuresis - [PE] (Physiologic Effect)
  • Vasoconstriction - [PE] (Physiologic Effect)
  • Vasopressins - [CS]
    • Sample Package:
    No
    FDA Application Number:
    NDA217569
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    09-29-2023
    Listing Expiration Date:
    12-31-2025
    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.

    Frequently Asked Questions

    What is NDC 0338-9647-12?

    The NDC Packaged Code 0338-9647-12 is assigned to a package of 12 bag in 1 carton / 100 ml in 1 bag of Vasopressin In 0.9% Sodium Chloride, a human prescription drug labeled by Baxter Healthcare Corporation. The product's dosage form is injection and is administered via intravenous form.

    Is NDC 0338-9647 included in the NDC Directory?

    Yes, Vasopressin In 0.9% Sodium Chloride with product code 0338-9647 is active and included in the NDC Directory. The product was first marketed by Baxter Healthcare Corporation on September 29, 2023 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 0338-9647-12?

    The 11-digit format is 00338964712. 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
    4-4-20338-9647-125-4-200338-9647-12