NDC Package 67828-0000-1 Hyaluronate Sodium

Powder - View Billable Units, 11-Digit Format, RxNorm

Package Information
Other Packages
Frequently Asked Questions

Package Information

This product is an UNFINISHED DRUG part of the official NDC directory. Unfinished drugs include products like active ingredients some of which are used in bulk for further processing or compounding. The FDA requires a list of these drugs manufactured in a U.S. commercial distribution facility.

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:

67828-0000-1

Package Description:

100 g in 1 BOTTLE

Product Code:

67828-0000

Non-Proprietary Name:

Hyaluronate Sodium

Substance Name:

Hyaluronate Sodium

Usage Information:

This medication is used to protect skin ulcers, burns, or wounds from irritation so that the skin can heal properly. Some products are also used to help relieve itching and pain from various skin conditions. Hyaluronate is the same as a natural substance that is found in your body. It works by forming a protective layer over the affected area.

11-Digit NDC Billing Format:

67828000001

Product Type:

Bulk Ingredient

Labeler Name:

Bloomage Biotechnology Corp., Ltd.

Dosage Form:

Powder - An intimate mixture of dry, finely divided drugs and/or chemicals that may be intended for internal or external use.

Active Ingredient(s):

HYALURONATE SODIUM 1 g/g

Sample Package:

N/A

Marketing Category:

BULK INGREDIENT - A category specifying that a product is marketed as a bulk ingredient.

Start Marketing Date:

01-01-2014

Listing Expiration Date:

12-31-2024

Exclude Flag:

Unfinished Product:

Yes

Code Structure:

67828 - Bloomage Biotechnology Corp., Ltd.
- 67828-0000 -
  - 67828-0000-1 - 100 g in 1 BOTTLE

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 disclaimer below.

Other Product Packages

The following packages are also available for this product:

NDC Package Code	Package Description
67828-0000-0	50 g in 1 BOTTLE
67828-0000-2	200 g in 1 BOTTLE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 67828-0000-1?

The NDC Packaged Code 67828-0000-1 is assigned to an UNFINISHED drug package of 100 g in 1 bottle of Hyaluronate Sodium, a bulk ingredient labeled by Bloomage Biotechnology Corp., Ltd.. The product's dosage form is powder and is administered via form.

Is NDC 67828-0000 included in the NDC Directory?

Yes, Hyaluronate Sodium is an UNFINISHED PRODUCT with code 67828-0000 that is active and included in the NDC Directory. The product was first marketed by Bloomage Biotechnology Corp., Ltd. on January 01, 2014 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 67828-0000-1?

The 11-digit format is 67828000001. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 5-4-1 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format	10-Digit Original Code	11-Digit Format	11-Digit Code
5-4-1	67828-0000-1	5-4-2	67828-0000-01

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