Viscum Abietis 5 Liquid
NDC Package 48951-9302-1

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

Package Information

Viscum Abietis 5 liquids is directions: FOR ORAL USE. This formulation utilizes a liquid delivery system. Marketed by Uriel Pharmacy Inc., this product is identified by NDC 48951-9302.

Identification & Billing

NDC Package Code
48951-9302-1
Package Description
8 AMPULE in 1 BOX / 1 mL in 1 AMPULE
Product Code
11-Digit Billing Format
48951930201

Clinical Specifications

Proprietary Name
Viscum Abietis 5
Non-Proprietary Name
Viscum Abietis 5
Substance Name
Viscum Album Fruiting Top
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route
Oral - Administration to or by way of the mouth.
Usage Information
Directions: FOR ORAL USE.

Regulatory & Marketing

Labeler Name
Uriel Pharmacy Inc.
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
08-01-2014
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 48951-9302-1 identifies a specific commercial package of 8 ampule in 1 box / 1 ml in 1 ampule of Viscum Abietis 5, a human over the counter drug labeled by Uriel Pharmacy Inc.. This liquid is formulated for oral use and contains viscum album fruiting top 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 Uriel Pharmacy Inc. on August 01, 2014. The current certification is valid through December 31, 2027.

How is this Uriel Pharmacy Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 48951930201. 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)
48951-9302-1
11-Digit CMS (5-4-2)
48951-9302-01

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