Clobetasol Propionate Cream
NDC Package 51672-1297-2

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

Clobetasol Propionate cream is a medication used to treat a variety of skin conditions (e.g., eczema, psoriasis, dermatitis, allergies, rash). This formulation utilizes a cream delivery system. Marketed by Sun Pharmaceutical Industries, Inc., this product is identified by NDC 51672-1297 and is authorized under FDA application ANDA075633.

Identification & Billing

NDC Package Code
51672-1297-2
Package Description
1 TUBE in 1 CARTON / 30 g in 1 TUBE
Product Code
51672-1297
11-Digit Billing Format
51672129702
Billing Unit
GM - Billing unit of "gram" is used when a product is measured by its weight.
Units Per Package
30 GM
RxNorm Crosswalk
  • RxCUI: 1992281 - clobetasol propionate 0.05 % Emollient Base Topical Cream
  • RxCUI: 1992281 - Emollient clobetasol propionate 0.5 MG/ML Topical Cream

Clinical Specifications

Proprietary Name
Clobetasol Propionate
Non-Proprietary Name
Clobetasol Propionate
Substance Name
Clobetasol Propionate
Dosage Form
Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
Administration Route
Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Active Ingredient(s)
CLOBETASOL PROPIONATE .5 mg/g
Pharmacologic Class
Usage Information
This medication is used to treat a variety of skin conditions (e.g., eczema, psoriasis, dermatitis, allergies, rash). Clobetasol reduces the swelling, itching, and redness that can occur in these types of conditions. This medication is a very strong (super-high-potency) corticosteroid.

Regulatory & Marketing

Labeler Name
Sun Pharmaceutical Industries, Inc.
Product Type
Human Prescription Drug
FDA Application #
ANDA075633
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
05-17-2000
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (51672-1297). Click a package code to view its specific billing and regulatory data.

51672-1297-1
1 TUBE in 1 CARTON / 15 g in 1 TUBE
51672-1297-3
1 TUBE in 1 CARTON / 60 g in 1 TUBE

* 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 51672-1297-2 identifies a specific commercial package of 1 tube in 1 carton / 30 g in 1 tube of Clobetasol Propionate, a human prescription drug labeled by Sun Pharmaceutical Industries, Inc.. This cream is formulated for topical use and contains clobetasol propionate 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 Sun Pharmaceutical Industries, Inc. on May 17, 2000. The current certification is valid through December 31, 2026.

What are the primary indications for this medication?

This medication is used to treat a variety of skin conditions (e.g., eczema, psoriasis, dermatitis, allergies, rash). Clobetasol reduces the swelling, itching, and redness that can occur in these types of conditions. This medication is a very strong (super-high-potency) corticosteroid.

How is this Sun Pharmaceutical Industries, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 51672129702. Quantities are measured in per "gm or gram", products billed per gram are products measured by weight.. There are 30 total billable units per package. 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)
51672-1297-2
11-Digit CMS (5-4-2)
51672-1297-02

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