NDC Package 43598-405-16 Phytonadione Phytonadione

Injection, Emulsion Intramuscular; Intravenous; Subcutaneous - 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:
43598-405-16
Package Description:
25 AMPULE in 1 CARTON / 1 mL in 1 AMPULE (43598-405-11)
Product Code:
Proprietary Name:
Phytonadione 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:
43598040516
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 1670192 - phytonadione 10 MG in 1 ML Injection
  • RxCUI: 1670192 - 1 ML vitamin K1 10 MG/ML Injection
  • RxCUI: 1670192 - phytonadione 10 MG per 1 ML Injection
  • RxCUI: 1670192 - vitamin K 1 10 MG per 1 ML Injection
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Dr.reddy's Laboratories Inc
    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):
    Sample Package:
    No
    FDA Application Number:
    ANDA207719
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated 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.

    NDC HCPCS Crosswalk

    This crosswalk is intended to help the public understand which drug products (identified by NDCs) are assigned to which HCPCS billing codes.

    NDC 43598-405-16 HCPCS crosswalk information with package details and bill units information.

    NDC Billing CodeHCPCS CodeHCPCS Code Desc.DosagePackage SizePackage QuantityBillable UnitsBillable Units / Pkg
    43598040516J3430Vitamin k phytonadione inj1 MG12510250

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 43598-405-16?

    The NDC Packaged Code 43598-405-16 is assigned to a package of 25 ampule in 1 carton / 1 ml in 1 ampule (43598-405-11) of Phytonadione Phytonadione, a human prescription drug labeled by Dr.reddy's Laboratories Inc. The product's dosage form is injection, emulsion and is administered via intramuscular; intravenous; subcutaneous form.

    Is NDC 43598-405 included in the NDC Directory?

    Yes, Phytonadione Phytonadione with product code 43598-405 is active and included in the NDC Directory. The product was first marketed by Dr.reddy's Laboratories 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 NDC billing unit for package 43598-405-16?

    The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.

    What is the 11-digit format for NDC 43598-405-16?

    The 11-digit format is 43598040516. 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
    5-3-243598-405-165-4-243598-0405-16