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  5. NDC Package Code: 70700-331-24 Phytonadione

NDC Package 70700-331-24 Phytonadione

Injection, Emulsion Intramuscular; 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:
70700-331-24
Package Description:
5 TRAY in 1 CARTON / 5 AMPULE in 1 TRAY (70700-331-25) / 1 mL in 1 AMPULE
Product Code:
70700-331
Proprietary Name:
Phytonadione
Non-Proprietary Name:
Phytonadione
Substance Name:
Phytonadione
Usage Information:
Vitamin K is used to treat and prevent low levels of certain substances (blood clotting factors) that your body naturally produces. These substances help your blood to thicken and stop bleeding normally (such as after an accidental cut or injury). Low levels of blood clotting factors increase the risk for unusual bleeding. Low levels may be caused by certain medications (such as warfarin) or medical conditions (such as obstructive jaundice). Vitamin K helps to treat and prevent unusual bleeding by increasing the body's production of blood clotting factors.
11-Digit NDC Billing Format:
70700033124
Product Type:
Human Prescription Drug
Labeler Name:
Xiromed Llc
Dosage Form:
Injection, Emulsion - An emulsion consisting of a sterile, pyrogen-free preparation intended to be administered parenterally.
Administration Route(s):
  • Intramuscular - Administration within a muscle.
  • Intravenous - Administration within or into a vein or veins.
  • Subcutaneous - Administration beneath the skin; hypodermic. Synonymous with the term SUBDERMAL.
Active Ingredient(s):
PHYTONADIONE 10 mg/mL
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
ANDA217386
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
08-28-2025
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.

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 70700-331-24?

The NDC Packaged Code 70700-331-24 is assigned to a package of 5 tray in 1 carton / 5 ampule in 1 tray (70700-331-25) / 1 ml in 1 ampule of Phytonadione, a human prescription drug labeled by Xiromed Llc. The product's dosage form is injection, emulsion and is administered via intramuscular; intravenous; subcutaneous form.

Is NDC 70700-331 included in the NDC Directory?

Yes, Phytonadione with product code 70700-331 is active and included in the NDC Directory. The product was first marketed by Xiromed Llc on August 28, 2025 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 70700-331-24?

The 11-digit format is 70700033124. 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
5-3-270700-331-245-4-270700-0331-24