Ssangbi Tang Liquid
NDC Package 73442-0008-1

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

Package Information

Ssangbi Tang (galgeun-tang extract) liquids is take 1 pouch 3 times a day. This formulation utilizes a liquid delivery system. Marketed by I World Pharmaceutical Co., Ltd., this product is identified by NDC 73442-0008.

Identification & Billing

NDC Package Code
73442-0008-1
Package Description
80 mL in 1 POUCH
Product Code
11-Digit Billing Format
73442000801

Clinical Specifications

Proprietary Name
Ssangbi Tang
Non-Proprietary Name
Galgeun-tang Extract
Substance Name
Ginger; Perilla Frutescens Leaf; Pueraria Montana Var. Lobata Whole
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
Take 1 pouch 3 times a day

Regulatory & Marketing

Labeler Name
I World Pharmaceutical Co., Ltd.
Product Type
Human Otc 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
10-08-2019
Listing Expiration
12-31-2026
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 73442-0008-1 identifies a specific commercial package of 80 ml in 1 pouch of Ssangbi Tang, a human over the counter drug labeled by I World Pharmaceutical Co., Ltd.. This liquid is formulated for oral use and contains ginger; perilla frutescens leaf; pueraria montana var. lobata whole 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 I World Pharmaceutical Co., Ltd. on October 08, 2019. The current certification is valid through December 31, 2026.

How is this I World Pharmaceutical Co., Ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 73442000801. 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)
73442-0008-1
11-Digit CMS (5-4-2)
73442-0008-01

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