NDC Package 65372-1134-2 Alendronate Sodium

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:
65372-1134-2
Package Description:
20 kg in 1 DRUM
Product Code:
Non-Proprietary Name:
Alendronate Sodium
Substance Name:
Alendronate Sodium
Usage Information:
Alendronate is used to prevent and treat certain types of bone loss (osteoporosis) in adults. Osteoporosis causes bones to become thinner and break more easily. Your chance of developing osteoporosis increases as you age, after menopause, or if you are taking corticosteroid medications (such as prednisone) for a long time. This medication works by slowing bone loss. This effect helps maintain strong bones and reduce the risk of broken bones (fractures). Alendronate belongs to a class of drugs called bisphosphonates.
11-Digit NDC Billing Format:
65372113402
Product Type:
Bulk Ingredient
Labeler Name:
Jubilant Pharmova Limited
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):
Sample Package:
N/A
Marketing Category:
BULK INGREDIENT - A category specifying that a product is marketed as a bulk ingredient.
Start Marketing Date:
03-31-2009
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 65372-1134-2?

The NDC Packaged Code 65372-1134-2 is assigned to an UNFINISHED drug package of 20 kg in 1 drum of Alendronate Sodium, a bulk ingredient labeled by Jubilant Pharmova Limited. The product's dosage form is powder and is administered via form.

Is NDC 65372-1134 included in the NDC Directory?

Yes, Alendronate Sodium is an UNFINISHED PRODUCT with code 65372-1134 that is active and included in the NDC Directory. The product was first marketed by Jubilant Pharmova Limited on March 31, 2009 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 65372-1134-2?

The 11-digit format is 65372113402. 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 Format10-Digit Original Code11-Digit Format11-Digit Code
5-4-165372-1134-25-4-265372-1134-02