NDC Package 0075-8016-10 Lovenox

Enoxaparin Sodium Injection 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:
0075-8016-10
Package Description:
10 CELLO PACK in 1 CARTON / 1 SYRINGE in 1 CELLO PACK / .6 mL in 1 SYRINGE (0075-8016-01)
Product Code:
Proprietary Name:
Lovenox
Non-Proprietary Name:
Enoxaparin Sodium
Substance 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:
00075801610
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 854228 - enoxaparin sodium 30 MG in 0.3 ML Prefilled Syringe
  • RxCUI: 854228 - 0.3 ML enoxaparin sodium 100 MG/ML Prefilled Syringe
  • RxCUI: 854228 - 0.3 ML ENX sodium 100 MG/ML Prefilled Syringe
  • RxCUI: 854228 - enoxaparin sodium 30 MG per 0.3 ML Prefilled Syringe
  • RxCUI: 854232 - Lovenox 30 MG in 0.3 mL Prefilled Syringe
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Sanofi-aventis U.s. Llc
    Dosage Form:
    Injection - A sterile preparation intended for parenteral use; five distinct classes of injections exist as defined by the USP.
    Administration Route(s):
  • Subcutaneous - Administration beneath the skin; hypodermic. Synonymous with the term SUBDERMAL.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    NDA020164
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    03-29-1993
    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 0075-8016-10?

    The NDC Packaged Code 0075-8016-10 is assigned to a package of 10 cello pack in 1 carton / 1 syringe in 1 cello pack / .6 ml in 1 syringe (0075-8016-01) of Lovenox, a human prescription drug labeled by Sanofi-aventis U.s. Llc. The product's dosage form is injection and is administered via subcutaneous form.

    Is NDC 0075-8016 included in the NDC Directory?

    Yes, Lovenox with product code 0075-8016 is active and included in the NDC Directory. The product was first marketed by Sanofi-aventis U.s. Llc on March 29, 1993 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 0075-8016-10?

    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 0075-8016-10?

    The 11-digit format is 00075801610. 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 4-4-2 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
    4-4-20075-8016-105-4-200075-8016-10