Physicians Ez Use M-pred
NDC Package 76420-520-01

11-digit billing NDC: 76420052001 · Billing unit: EA · 1 EA per package
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

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

Physicians Ez Use M-pred is dEPO-MEDROL is contraindicated in patients with known hypersensitivity to the product and its constituents.Intramuscular corticosteroid preparations are contraindicated for idiopathic thrombocytopenic purpura.DEPO-MEDROL Sterile Aqueous Suspension is contraindicated for intrathecal administration. Marketed by Asclemed Usa, Inc., this product is identified by NDC 76420-520.

Identification & Billing

NDC Package Code
76420-520-01
Package Description
1 KIT in 1 CARTON * 10 mL in 1 VIAL, SINGLE-DOSE (0409-1162-18) * 100 PACKET in 1 BOX (53329-941-30) / 1 mL in 1 PACKET * 1 VIAL, MULTI-DOSE in 1 CARTON (0781-3522-75) / 5 mL in 1 VIAL, MULTI-DOSE
Product Code
76420-520
11-Digit Billing Format
76420052001
Billing Unit
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
Units Per Package
1 EA

Clinical Specifications

Proprietary Name
Physicians Ez Use M-pred
Dosage Form
-
Usage Information
DEPO-MEDROL is contraindicated in patients with known hypersensitivity to the product and its constituents.Intramuscular corticosteroid preparations are contraindicated for idiopathic thrombocytopenic purpura.DEPO-MEDROL Sterile Aqueous Suspension is contraindicated for intrathecal administration. Reports of severe medical events have been associated with this route of administration. DEPO-MEDROL is contraindicated for use in premature infants because the formulation contains benzyl alcohol. (See WARNINGS and PRECAUTIONS: Pediatric Use.) DEPO-MEDROL is contraindicated in systemic fungal infections, except when administered as an intra-articular injection for localized joint conditions (see WARNINGS: Infections, Fungal Infections). MARCAINE is contraindicated in obstetrical paracervical block anesthesia. Its use in this technique has resulted in fetal bradycardia and death.MARCAINE is contraindicated in patients with a known hypersensitivity to it or to any local anesthetic agent of the amide-type or to other components of MARCAINE solutions.

Regulatory & Marketing

Labeler Name
Asclemed Usa, Inc.
Marketing Category
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date
05-30-2013
End Marketing Date
06-30-2026
Listing Expiration
06-30-2026
Exclude Flag
D
Sample Package
No

Hierarchy Structure

Code Lineage

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 76420-520-01 identifies a specific commercial package of 1 kit in 1 carton * 10 ml in 1 vial, single-dose (0409-1162-18) * 100 packet in 1 box (53329-941-30) / 1 ml in 1 packet * 1 vial, multi-dose in 1 carton (0781-3522-75) / 5 ml in 1 vial, multi-dose of Physicians Ez Use M-pred, labeled by Asclemed Usa, Inc.. This product is billed for "EA" each discreet unit and contains an estimated amount of 1 billable units per package. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Asclemed Usa, Inc. on May 30, 2013. The current certification is valid through June 30, 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: 76420052001. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 1 total billable units per package. 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:

10-Digit Format (5-3-2)
76420-520-01
11-Digit CMS (5-4-2)
76420-0520-01

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.