Solep Premier Hi Gro Ampoule Pack
NDC Package 81077-030-02

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.

Solep Premier Hi Gro Ampoule Pack is ■ Shake the product before use, daily apply adequate amount and gently massage the scalp with fingertips to be fully absorbed. Marketed by Kobizstar Co., Ltd., this product is identified by NDC 81077-030.

Identification & Billing

NDC Package Code
81077-030-02
Package Description
1 TUBE in 1 CARTON / 40 mL in 1 TUBE (81077-030-01)
Product Code
81077-030
11-Digit Billing Format
81077003002

Clinical Specifications

Proprietary Name
Solep Premier Hi Gro Ampoule Pack
Dosage Form
-
Usage Information
■ Shake the product before use, daily apply adequate amount and gently massage the scalp with fingertips to be fully absorbed.

Regulatory & Marketing

Labeler Name
Kobizstar Co., Ltd.
Marketing Category
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date
11-01-2020
Listing Expiration
12-31-2024
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 81077-030-02 identifies a specific commercial package of 1 tube in 1 carton / 40 ml in 1 tube (81077-030-01) of Solep Premier Hi Gro Ampoule Pack, labeled by Kobizstar Co., Ltd.. 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 Kobizstar Co., Ltd. on November 01, 2020. The current certification is valid through December 31, 2024.

How is this Kobizstar Co., Ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 81077003002. 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)
81077-030-02
11-Digit CMS (5-4-2)
81077-0030-02

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