Multi-specialty Kit
NDC Package 63187-350-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
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 inactivated by the FDA.

Multi-specialty Kit is dEPO-MEDROL is contraindicated in patients with known hypersensitivity to the product and its constituents. Marketed by Proficient Rx Lp, this product is identified by NDC 63187-350 and is authorized under FDA application NDA011757.

Identification & Billing

NDC Package Code
63187-350-01
Package Description
1 KIT in 1 CARTON * 2 mL in 1 AMPULE (0409-4713-32) * 5 mL in 1 POUCH (53329-820-09) * 1 VIAL, SINGLE-DOSE in 1 PACKAGE (0009-3073-01) / 1 mL in 1 VIAL, SINGLE-DOSE
Product Code
63187-350
11-Digit Billing Format
63187035001
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
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 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
Proficient Rx Lp
FDA Application #
NDA011757
Marketing Category
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date
02-06-2014
Listing Expiration
12-31-2017
Exclude Flag
I
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 63187-350-01 identifies a specific commercial package of 1 kit in 1 carton * 2 ml in 1 ampule (0409-4713-32) * 5 ml in 1 pouch (53329-820-09) * 1 vial, single-dose in 1 package (0009-3073-01) / 1 ml in 1 vial, single-dose of Multi-specialty Kit, labeled by Proficient Rx Lp. 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 Proficient Rx Lp on February 06, 2014. The current certification is valid through December 31, 2017.

How is this Proficient Rx Lp product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 63187035001. 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)
63187-350-01
11-Digit CMS (5-4-2)
63187-0350-01

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