NDC Package 65841-101-12 Atenolol

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:
65841-101-12
Package Description:
1 BAG in 1 DRUM / 1 BAG in 1 BAG / 1 BAG in 1 BAG / 35 kg in 1 BAG
Product Code:
Non-Proprietary Name:
Atenolol
Substance Name:
Atenolol
Usage Information:
Atenolol is used with or without other medications to treat high blood pressure (hypertension). Lowering high blood pressure helps prevent strokes, heart attacks, and kidney problems. This medication is also used to treat chest pain (angina) and to improve survival after a heart attack. Atenolol belongs to a class of drugs known as beta blockers. It works by blocking the action of certain natural chemicals in your body, such as epinephrine, on the heart and blood vessels. This effect lowers the heart rate, blood pressure, and strain on the heart.
11-Digit NDC Billing Format:
65841010112
Product Type:
Bulk Ingredient
Labeler Name:
Zydus Lifesciences 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:
01-11-2018
Listing Expiration Date:
12-31-2025
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 65841-101-12?

The NDC Packaged Code 65841-101-12 is assigned to an UNFINISHED drug package of 1 bag in 1 drum / 1 bag in 1 bag / 1 bag in 1 bag / 35 kg in 1 bag of Atenolol, a bulk ingredient labeled by Zydus Lifesciences Limited. The product's dosage form is powder and is administered via form.

Is NDC 65841-101 included in the NDC Directory?

Yes, Atenolol is an UNFINISHED PRODUCT with code 65841-101 that is active and included in the NDC Directory. The product was first marketed by Zydus Lifesciences Limited on January 11, 2018 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 65841-101-12?

The 11-digit format is 65841010112. 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
5-3-265841-101-125-4-265841-0101-12