NDC Package 71093-142-05 Clopidogrel Bisulfate

View Billable Units, 11-Digit Format, RxNorm

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
71093-142-05
Package Description:
500 TABLET, FILM COATED in 1 BOTTLE
Product Code:
Proprietary Name:
Clopidogrel Bisulfate
Usage Information:
Clopidogrel tablets are indicated to reduce the rate of myocardial infarction (MI) and stroke in patients with non–ST-segment elevation ACS (unstable angina [UA]/non–ST-elevation myocardial infarction [NSTEMI]), including patients who are to be managed medically and those who are to be managed with coronary revascularization. Clopidogrel tablets should be administered in conjunction with aspirin.Clopidogrel tablets are indicated to reduce the rate of myocardial infarction and stroke in patients with acute ST-elevation myocardial infarction (STEMI) who are to be managed medically. Clopidogrel should be administered in conjunction with aspirin.
11-Digit NDC Billing Format:
71093014205
NDC to RxNorm Crosswalk:
Labeler Name:
Aci Healthcare Usa, Inc
Sample Package:
No
FDA Application Number:
ANDA078004
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
07-01-2022
Listing Expiration Date:
12-31-2024
Exclude Flag:
I
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
71093-142-0490 TABLET, FILM COATED in 1 BOTTLE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 71093-142-05?

The NDC Packaged Code 71093-142-05 is assigned to a package of 500 tablet, film coated in 1 bottle of Clopidogrel Bisulfate, labeled by Aci Healthcare Usa, Inc. The product's dosage form is and is administered via form.

Is NDC 71093-142 included in the NDC Directory?

No, Clopidogrel Bisulfate with product code 71093-142 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Aci Healthcare Usa, Inc on July 01, 2022 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 71093-142-05?

The 11-digit format is 71093014205. 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
5-3-271093-142-055-4-271093-0142-05