NDC Package 48246-100-10 Hydrocortisone Probutate

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:

48246-100-10

Package Description:

1 kg in 1 DRUM

Product Code:

48246-100

Non-Proprietary Name:

Hydrocortisone Probutate

Substance Name:

Hydrocortisone Probutate

Usage Information:

This medication is used to treat a variety of skin conditions (e.g., eczema, dermatitis, allergies, rash). Hydrocortisone probutate reduces the swelling, itching, and redness that can occur in these types of conditions. This medication is a medium-strength corticosteroid. Do not use this medication to treat diaper rash.

11-Digit NDC Billing Format:

48246010010

Product Type:

Bulk Ingredient

Labeler Name:

Taisho Pharmaceutical Co., 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):

HYDROCORTISONE PROBUTATE 2 kg/2kg

Sample Package:

N/A

Marketing Category:

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

Start Marketing Date:

08-29-1996

Listing Expiration Date:

12-31-2025

Exclude Flag:

Unfinished Product:

Yes

Code Structure:

48246 - Taisho Pharmaceutical Co., Ltd.
- 48246-100 -
  - 48246-100-10 - 1 kg in 1 DRUM

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
48246-100-01	.1 kg in 1 CAN
48246-100-03	.3 kg in 1 CAN
48246-100-05	.5 kg in 1 DRUM
48246-100-20	2 kg in 1 DRUM

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 48246-100-10?

The NDC Packaged Code 48246-100-10 is assigned to an UNFINISHED drug package of 1 kg in 1 drum of Hydrocortisone Probutate, a bulk ingredient labeled by Taisho Pharmaceutical Co., Ltd.. The product's dosage form is powder and is administered via form.

Is NDC 48246-100 included in the NDC Directory?

Yes, Hydrocortisone Probutate is an UNFINISHED PRODUCT with code 48246-100 that is active and included in the NDC Directory. The product was first marketed by Taisho Pharmaceutical Co., Ltd. on August 29, 1996 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 48246-100-10?

The 11-digit format is 48246010010. 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 5-3-2 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
5-3-2	48246-100-10	5-4-2	48246-0100-10

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