NDC Package 70771-1318-4 Phytonadione

Tablet Oral - 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:
70771-1318-4
Package Description:
10 BLISTER PACK in 1 CARTON / 10 TABLET in 1 BLISTER PACK (70771-1318-2)
Product Code:
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:
70771131804
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:
    Zydus Lifesciences Limited
    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):
    Sample Package:
    No
    FDA Application Number:
    ANDA210189
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    02-22-2019
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    70771-1318-11 BOTTLE in 1 CARTON / 100 TABLET in 1 BOTTLE
    70771-1318-330 TABLET in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 70771-1318-4?

    The NDC Packaged Code 70771-1318-4 is assigned to a package of 10 blister pack in 1 carton / 10 tablet in 1 blister pack (70771-1318-2) of Phytonadione, a human prescription drug labeled by Zydus Lifesciences Limited. The product's dosage form is tablet and is administered via oral form.

    Is NDC 70771-1318 included in the NDC Directory?

    Yes, Phytonadione with product code 70771-1318 is active and included in the NDC Directory. The product was first marketed by Zydus Lifesciences Limited on February 22, 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 11-digit format for NDC 70771-1318-4?

    The 11-digit format is 70771131804. 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 5-4-1 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
    5-4-170771-1318-45-4-270771-1318-04