Physicians Ez Use M-pred Kit
NDC Package 76420-216-01

11-digit billing NDC: 76420021601
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Physicians Ez Use M-pred (bupivacaine hydrochloride, methylprednisolone acetate, povidone-iodine) kits is bupivacaine Hydrochloride Injection is indicated in adults for the production of local or regional anesthesia or analgesia for surgery, dental and oral surgery procedures, diagnostic and therapeutic procedures, and for obstetrical procedures. This formulation utilizes a kit delivery system. Marketed by Asclemed Usa, Inc., this product is identified by NDC 76420-216.

Identification & Billing

NDC Package Code
76420-216-01
Package Description
1 KIT in 1 CARTON * 25 VIAL, SINGLE-DOSE in 1 CARTON (70121-1573-2) / 1 mL in 1 VIAL, SINGLE-DOSE * 100 PACKET in 1 BOX (53329-941-30) / 1 mL in 1 PACKET (53329-941-09) * 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-1162-01) / 10 mL in 1 VIAL, SINGLE-DOSE (0409-1162-18)
Product Code
76420-216
11-Digit Billing Format
76420021601

Clinical Specifications

Proprietary Name
Physicians Ez Use M-pred
Non-Proprietary Name
Bupivacaine Hydrochloride, Methylprednisolone Acetate, Povidone-iodine
Dosage Form
Kit - A packaged collection of related material.
Administration Route
  • Epidural - Administration upon or over the dura mater.
  • Infiltration - Administration that results in substances passing into tissue spaces or into cells.
  • Intramuscular - Administration within a muscle.
  • Intrasynovial - Administration within the synovial cavity of a joint.
  • Soft Tissue - Administration into any soft tissue.
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Usage Information
Bupivacaine Hydrochloride Injection is indicated in adults for the production of local or regional anesthesia or analgesia for surgery, dental and oral surgery procedures, diagnostic and therapeutic procedures, and for obstetrical procedures. Specific concentrations and presentations of Bupivacaine Hydrochloride Injection are recommended for each type of block indicated to produce local or regional anesthesia or analgesia [see Dosage and Administration (2.2)].

Regulatory & Marketing

Labeler Name
Asclemed Usa, Inc.
Product Type
Human Prescription Drug
Marketing Category
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date
09-25-2026
Listing Expiration
12-31-2027
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage
  • 76420 - Asclemed Usa, Inc.
    • 76420-216 - Physicians Ez Use M-pred
      • 76420-216-01 - 1 KIT in 1 CARTON * 25 VIAL, SINGLE-DOSE in 1 CARTON (70121-1573-2) / 1 mL in 1 VIAL, SINGLE-DOSE * 100 PACKET in 1 BOX (53329-941-30) / 1 mL in 1 PACKET (53329-941-09) * 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-1162-01) / 10 mL in 1 VIAL, SINGLE-DOSE (0409-1162-18)

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 76420-216-01 identifies a specific commercial package of 1 kit in 1 carton * 25 vial, single-dose in 1 carton (70121-1573-2) / 1 ml in 1 vial, single-dose * 100 packet in 1 box (53329-941-30) / 1 ml in 1 packet (53329-941-09) * 25 vial, single-dose in 1 tray (0409-1162-01) / 10 ml in 1 vial, single-dose (0409-1162-18) of Physicians Ez Use M-pred, a human prescription drug labeled by Asclemed Usa, Inc.. This kit is formulated for epidural; infiltration; intramuscular; intrasynovial; soft tissue; 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 September 25, 2026. The current certification is valid through December 31, 2027.

How is this Asclemed Usa, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 76420021601. 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)
76420-216-01
11-Digit CMS (5-4-2)
76420-0216-01

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