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  5. NDC Package Code: 72843-461-10 Desmopressin Acetate

NDC Package 72843-461-10 Desmopressin Acetate

Injection Intravenous; Subcutaneous - 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:
72843-461-10
Package Description:
10 VIAL in 1 CARTON / 1 mL in 1 VIAL
Product Code:
72843-461
Proprietary Name:
Desmopressin Acetate
Non-Proprietary Name:
Desmopressin Acetate
Substance Name:
Desmopressin Acetate
Usage Information:
Desmopressin is used to control the amount of urine your kidneys make. Normally, the amount of urine you make is controlled by a certain substance in the body called vasopressin. In people who have "water diabetes" (diabetes insipidus) or certain kinds of head injury or brain surgery, the body does not make enough vasopressin. Desmopressin is a man-made form of vasopressin and is used to replace a low level of vasopressin. This medication helps to control increased thirst and too much urination due to these conditions, and helps prevent dehydration. Desmopressin products applied in the nose are no longer indicated to control nighttime bedwetting in children because of the increased risk of developing a serious side effect (a low level of sodium in the blood).
11-Digit NDC Billing Format:
72843046110
NDC to RxNorm Crosswalk:
Product Type:
Human Prescription Drug
Labeler Name:
Ubi Pharma Inc.
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.
  • Subcutaneous - Administration beneath the skin; hypodermic. Synonymous with the term SUBDERMAL.
Active Ingredient(s):
DESMOPRESSIN ACETATE 4 ug/mL
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
ANDA210223
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
09-17-2020
Listing Expiration Date:
12-31-2026
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.

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Frequently Asked Questions

What is NDC 72843-461-10?

The NDC Packaged Code 72843-461-10 is assigned to a package of 10 vial in 1 carton / 1 ml in 1 vial of Desmopressin Acetate, a human prescription drug labeled by Ubi Pharma Inc.. The product's dosage form is injection and is administered via intravenous; subcutaneous form.

Is NDC 72843-461 included in the NDC Directory?

Yes, Desmopressin Acetate with product code 72843-461 is active and included in the NDC Directory. The product was first marketed by Ubi Pharma Inc. on September 17, 2020 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 72843-461-10?

The 11-digit format is 72843046110. 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
5-3-272843-461-105-4-272843-0461-10