Multi-specialty Kit
NDC Package 76420-780-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

Multi-specialty Kit (depo-medrol, lidocaine, isopropyl alcohol) kits is dEPO-MEDROL is contraindicated in patients with known hypersensitivity to the product and its constituents. This formulation utilizes a kit delivery system. Marketed by Asclemed Usa, Inc., this product is identified by NDC 76420-780.

Identification & Billing

NDC Package Code
76420-780-01
Package Description
1 KIT in 1 CARTON * 10 AMPULE in 1 CARTON (55150-158-72) / 2 mL in 1 AMPULE * 5 mL in 1 POUCH * 25 VIAL, SINGLE-DOSE in 1 CARTON (70121-1573-5) / 1 mL in 1 VIAL, SINGLE-DOSE
Product Code
11-Digit Billing Format
76420078001
Billing Unit
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Multi-specialty Kit
Non-Proprietary Name
Depo-medrol, Lidocaine, Isopropyl Alcohol
Dosage Form
Kit - A packaged collection of related material.
Administration Route
  • Infiltration - Administration that results in substances passing into tissue spaces or into cells.
  • Intra-articular - Administration within a joint.
  • Intralesional - Administration within or introduced directly into a localized lesion.
  • Intramuscular - Administration within a muscle.
  • 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
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 is contraindicated for intrathecal administration. This formulation of methylprednisolone acetate has been associated with reports of severe medical events when administered by this route. 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). Lidocaine is contraindicated in patients with a known history of hypersensitivity to local anesthetics of the amide type.

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
02-06-2014
Listing Expiration
12-31-2027
Exclude Flag
N
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 76420-780-01 identifies a specific commercial package of 1 kit in 1 carton * 10 ampule in 1 carton (55150-158-72) / 2 ml in 1 ampule * 5 ml in 1 pouch * 25 vial, single-dose in 1 carton (70121-1573-5) / 1 ml in 1 vial, single-dose of Multi-specialty Kit, a human prescription drug labeled by Asclemed Usa, Inc.. This kit is formulated for infiltration; intra-articular; intralesional; intramuscular; 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 February 06, 2014. 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: 76420078001. 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:

10-Digit Format (5-3-2)
76420-780-01
11-Digit CMS (5-4-2)
76420-0780-01

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