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  5. NDC Package Code: 72134-008-01 Phytonadione

NDC Package 72134-008-01 Phytonadione

Tablet Oral - 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:
72134-008-01
Package Description:
100 TABLET in 1 BOTTLE
Product Code:
72134-008
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:
72134000801
NDC to RxNorm Crosswalk:
  • RxCUI: 198102 - phytonadione 5 MG Oral Tablet
  • RxCUI: 198102 - vitamin K1 5 MG Oral Tablet
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Agnitio Inc.
    Dosage Form:
    Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • PHYTONADIONE 5 mg/1
    • Pharmacologic Class(es):
  • Increased Prothrombin Activity - [PE] (Physiologic Effect)
  • Reversed Anticoagulation Activity - [PE] (Physiologic Effect)
  • Vitamin K - [CS]
  • Vitamin K - [EPC] (Established Pharmacologic Class)
  • Warfarin Reversal Agent - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    ANDA213336
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    02-11-2022
    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.

    Frequently Asked Questions

    What is NDC 72134-008-01?

    The NDC Packaged Code 72134-008-01 is assigned to a package of 100 tablet in 1 bottle of Phytonadione, a human prescription drug labeled by Agnitio Inc.. The product's dosage form is tablet and is administered via oral form.

    Is NDC 72134-008 included in the NDC Directory?

    Yes, Phytonadione with product code 72134-008 is active and included in the NDC Directory. The product was first marketed by Agnitio Inc. on February 11, 2022 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 72134-008-01?

    The 11-digit format is 72134000801. 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
    5-3-272134-008-015-4-272134-0008-01