Enoxiluv Kit
NDC Package 76420-532-01
Package Information
Enoxiluv Kit (enoxaparin sodium, isopropyl alcohol) kits is enoxaparin sodium injection is contraindicated in patients with:Active major bleeding. This formulation utilizes a kit delivery system. Marketed by Asclemed Usa, Inc., this product is identified by NDC 76420-532.
Identification & Billing
- RxCUI: 797544 - isopropyl alcohol 70 % Medicated Pad
- RxCUI: 797544 - isopropyl alcohol 0.7 ML/ML Medicated Pad
- RxCUI: 797544 - isopropyl alcohol 70 % Topical Cloth
- RxCUI: 797544 - isopropyl alcohol 70 % Topical Swab
- RxCUI: 854235 - enoxaparin sodium 40 MG in 0.4 ML Prefilled Syringe
Clinical Specifications
- Subcutaneous - Administration beneath the skin; hypodermic. Synonymous with the term SUBDERMAL.
- Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Regulatory & Marketing
Hierarchy Structure
- 76420 - Asclemed Usa, Inc.
- 76420-532 - Enoxiluv Kit
- 76420-532-01 - 1 KIT in 1 CARTON * 10 SYRINGE in 1 CARTON (0781-3246-64) / .4 mL in 1 SYRINGE * 5 mL in 1 POUCH
- 76420-532 - Enoxiluv Kit
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 full disclaimer at the bottom of this page.
Frequently Asked Questions
What is the distribution configuration for this product package?
The code 76420-532-01 identifies a specific commercial package of 1 kit in 1 carton * 10 syringe in 1 carton (0781-3246-64) / .4 ml in 1 syringe * 5 ml in 1 pouch of Enoxiluv Kit, a human prescription drug labeled by Asclemed Usa, Inc.. This kit is formulated for subcutaneous; topical use and contains as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Asclemed Usa, Inc. on February 08, 2023. The current certification is valid through December 31, 2026.
How is this Asclemed Usa, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 76420053201. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.