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  5. NDC Package Code: 68682-170-30 Phytonadione

NDC Package 68682-170-30 Phytonadione

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

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:
68682-170-30
Package Description:
1 BOTTLE in 1 CARTON / 30 TABLET in 1 BOTTLE
Product Code:
68682-170
Proprietary 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:
68682017030
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
1 EA
Labeler Name:
Oceanside Pharmaceuticals
Sample Package:
No
FDA Application Number:
NDA010104
Marketing Category:
NDA AUTHORIZED GENERIC - A product marketed as a "generic" drug under an approved New Drug Application (NDA), rather than an Abbreviated New Drug Application (ANDA),.
Start Marketing Date:
04-23-2018
End Marketing Date:
10-01-2022
Listing Expiration Date:
10-01-2022
Exclude Flag:
D
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
68682-170-051 BOTTLE in 1 CARTON / 100 TABLET in 1 BOTTLE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 68682-170-30?

The NDC Packaged Code 68682-170-30 is assigned to a package of 1 bottle in 1 carton / 30 tablet in 1 bottle of Phytonadione, labeled by Oceanside Pharmaceuticals. The product's dosage form is and is administered via form.

Is NDC 68682-170 included in the NDC Directory?

No, Phytonadione with product code 68682-170 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Oceanside Pharmaceuticals on April 23, 2018 and its listing in the NDC Directory is set to expire on October 01, 2022 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 68682-170-30?

The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 1.

What is the 11-digit format for NDC 68682-170-30?

The 11-digit format is 68682017030. 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
5-3-268682-170-305-4-268682-0170-30