Morphinum
NDC Package 10191-1013-2

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.

Morphinum is nAUSEOUS STOMACH, POSITIONAL VERTIGO, MULTIPLE NEURITIS, OR OTHER INDICATIONS. Marketed by Remedy Makers, this product is identified by NDC 10191-1013.

Identification & Billing

NDC Package Code
10191-1013-2
Package Description
151 PELLET in 1 VIAL, GLASS
Product Code
10191-1013
11-Digit Billing Format
10191101302

Clinical Specifications

Proprietary Name
Morphinum
Dosage Form
-
Usage Information
NAUSEOUS STOMACH, POSITIONAL VERTIGO, MULTIPLE NEURITIS, OR OTHER INDICATIONS. INDICATIONS: To be use according to standard homeopathic indications,or as prescribed by a licensed physician. Free from yeast, wheat, corn, and soy.

Regulatory & Marketing

Labeler Name
Remedy Makers
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
04-27-2001
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 10191-1013-2 identifies a specific commercial package of 151 pellet in 1 vial, glass of Morphinum, labeled by Remedy Makers. 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 Remedy Makers on April 27, 2001. The current certification is valid through December 31, 2017.

How is this Remedy Makers product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 10191101302. 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 (5-4-1)
10191-1013-2
11-Digit CMS (5-4-2)
10191-1013-02

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