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  5. NDC Package Code: 62037-839-20 Enoxaparin Sodium

NDC Package 62037-839-20 Enoxaparin Sodium

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory .

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:
62037-839-20
Package Description:
10 BLISTER PACK in 1 CARTON / 1 SYRINGE in 1 BLISTER PACK / .3 mL in 1 SYRINGE
Product Code:
62037-839
Proprietary Name:
Enoxaparin Sodium
Usage Information:
Enoxaparin is used to prevent and treat harmful blood clots. This helps to reduce the risk of a stroke or heart attack. This medication helps keep your blood flowing smoothly by lowering the activity of clotting proteins in the blood. Enoxaparin is an anticoagulant, also known as a "blood thinner." It is a type of heparin. Conditions which increase your risk of developing blood clots include certain types of surgeries (such as knee/hip replacement, abdominal), long periods of being immobile, certain types of heart attack, and a specific type of chest pain called unstable angina. For some medical conditions, enoxaparin may be used in combination with other "blood thinners."
11-Digit NDC Billing Format:
62037083920
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
Labeler Name:
Actavis Pharma, Inc.
Sample Package:
No
FDA Application Number:
ANDA076684
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
01-27-2012
End Marketing Date:
05-31-2018
Listing Expiration Date:
05-31-2018
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.

Frequently Asked Questions

What is NDC 62037-839-20?

The NDC Packaged Code 62037-839-20 is assigned to a package of 10 blister pack in 1 carton / 1 syringe in 1 blister pack / .3 ml in 1 syringe of Enoxaparin Sodium, labeled by Actavis Pharma, Inc.. The product's dosage form is and is administered via form.

Is NDC 62037-839 included in the NDC Directory?

The product was first marketed by Actavis Pharma, Inc. on January 27, 2012 and its listing in the NDC Directory is set to expire on May 31, 2018 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 62037-839-20?

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 62037-839-20?

The 11-digit format is 62037083920. 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
5-3-262037-839-205-4-262037-0839-20