NDC Package 59651-398-37 Clopidogrel Bisulfate (form Ii)

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:
59651-398-37
Package Description:
50 kg in 1 DRUM
Product Code:
Non-Proprietary Name:
Clopidogrel Bisulfate (form Ii)
Substance Name:
Clopidogrel Bisulfate
Usage Information:
Clopidogrel is used to prevent heart attacks and strokes in persons with heart disease (recent heart attack), recent stroke, or blood circulation disease (peripheral vascular disease). It is also used with aspirin to treat new/worsening chest pain (new heart attack, unstable angina) and to keep blood vessels open and prevent blood clots after certain procedures (such as cardiac stent). Clopidogrel works by blocking platelets from sticking together and prevents them from forming harmful clots. It is an antiplatelet drug. It helps keep blood flowing smoothly in your body.
11-Digit NDC Billing Format:
59651039837
Product Type:
Bulk Ingredient
Labeler Name:
Aurobindo Pharma 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:
01-11-2024
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 59651-398-37?

The NDC Packaged Code 59651-398-37 is assigned to an UNFINISHED drug package of 50 kg in 1 drum of Clopidogrel Bisulfate (form Ii), a bulk ingredient labeled by Aurobindo Pharma Limited. The product's dosage form is powder and is administered via form.

Is NDC 59651-398 included in the NDC Directory?

Yes, Clopidogrel Bisulfate (form Ii) is an UNFINISHED PRODUCT with code 59651-398 that is active and included in the NDC Directory. The product was first marketed by Aurobindo Pharma Limited on January 11, 2024 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 59651-398-37?

The 11-digit format is 59651039837. 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
5-3-259651-398-375-4-259651-0398-37