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  5. NDC Package Code: 46708-707-50 Clobetasol Propionate

NDC Package 46708-707-50 Clobetasol Propionate

Aerosol, Foam Topical - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

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:
46708-707-50
Package Description:
1 CAN in 1 CARTON / 50 g in 1 CAN
Product Code:
46708-707
Proprietary Name:
Clobetasol Propionate
Non-Proprietary Name:
Clobetasol Propionate
Substance Name:
Clobetasol Propionate
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.
11-Digit NDC Billing Format:
46708070750
NDC to RxNorm Crosswalk:
Product Type:
Human Prescription Drug
Labeler Name:
Alembic Pharmaceuticals Limited
Dosage Form:
Aerosol, Foam - A dosage form containing one or more active ingredients, surfactants, aqueous or nonaqueous liquids, and the propellants; if the propellant is in the internal (discontinuous) phase (i.e., of the oil-in-water type), a stable foam is discharged, and if the propellant is in the external (continuous) phase (i.e., of the water-in-oil type), a spray or a quick-breaking foam is discharged.
Administration Route(s):
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(es):
Sample Package:
No
FDA Application Number:
ANDA215838
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
04-25-2025
Listing Expiration Date:
12-31-2026
Exclude Flag:
N
Code Structure:

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 CodePackage Description
46708-707-311 CAN in 1 CARTON / 100 g in 1 CAN

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 46708-707-50?

The NDC Packaged Code 46708-707-50 is assigned to a package of 1 can in 1 carton / 50 g in 1 can of Clobetasol Propionate, a human prescription drug labeled by Alembic Pharmaceuticals Limited. The product's dosage form is aerosol, foam and is administered via topical form.

Is NDC 46708-707 included in the NDC Directory?

Yes, Clobetasol Propionate with product code 46708-707 is active and included in the NDC Directory. The product was first marketed by Alembic Pharmaceuticals Limited on April 25, 2025 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 46708-707-50?

The 11-digit format is 46708070750. 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 Format10-Digit Original Code11-Digit Format11-Digit Code
5-3-246708-707-505-4-246708-0707-50