NDC Package 52128-167-01 Beclomethasone Dipropionate

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

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:
52128-167-01
Package Description:
1 kg in 1 CONTAINER
Product Code:
Non-Proprietary Name:
Beclomethasone Dipropionate
Substance Name:
Beclomethasone Dipropionate
Usage Information:
Beclomethasone is used to prevent and treat seasonal and year-round allergy symptoms (such as stuffy/runny nose, itchy eyes/nose/throat, sneezing). It may be used to treat symptoms (such as stuffy/runny nose) caused by other triggers (such as cigarette smoke, perfumes). It is also used to prevent the return of growths in the nose (nasal polyps) after removal by surgery. Beclomethasone belongs to a class of drugs known as corticosteroids. It works by reducing swelling (inflammation) in the nasal passages.
11-Digit NDC Billing Format:
52128016701
Product Type:
Bulk Ingredient
Labeler Name:
Symbiotica Speciality Ingredients Sdn.bhd
Dosage Form:
Powder - An intimate mixture of dry, finely divided drugs and/or chemicals that may be intended for internal or external use.
Sample Package:
N/A
Marketing Category:
BULK INGREDIENT - A category specifying that a product is marketed as a bulk ingredient.
Start Marketing Date:
03-20-2013
Listing Expiration Date:
12-31-2024
Exclude Flag:
N
Unfinished Product:
Yes
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.

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Frequently Asked Questions

What is NDC 52128-167-01?

The NDC Packaged Code 52128-167-01 is assigned to an UNFINISHED drug package of 1 kg in 1 container of Beclomethasone Dipropionate, a bulk ingredient labeled by Symbiotica Speciality Ingredients Sdn.bhd. The product's dosage form is powder and is administered via form.

Is NDC 52128-167 included in the NDC Directory?

Yes, Beclomethasone Dipropionate is an UNFINISHED PRODUCT with code 52128-167 that is active and included in the NDC Directory. The product was first marketed by Symbiotica Speciality Ingredients Sdn.bhd on March 20, 2013 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 52128-167-01?

The 11-digit format is 52128016701. 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
5-3-252128-167-015-4-252128-0167-01