NDC Package 0024-1332-30 Plavix

Clopidogrel Tablet, Film Coated Oral - View Billable Units, 11-Digit Format, RxNorm

Package Information

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:
0024-1332-30
Package Description:
3 BLISTER PACK in 1 CARTON / 10 TABLET, FILM COATED in 1 BLISTER PACK
Product Code:
Proprietary Name:
Plavix
Non-Proprietary Name:
Clopidogrel
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:
00024133230
NDC to RxNorm Crosswalk:
  • RxCUI: 213169 - Plavix 75 MG Oral Tablet
  • RxCUI: 213169 - clopidogrel 75 MG Oral Tablet [Plavix]
  • RxCUI: 213169 - Plavix 75 MG (clopidogrel bisulfate 97.875 MG) Oral Tablet
  • RxCUI: 309362 - clopidogrel 75 MG Oral Tablet
  • RxCUI: 309362 - clopidogrel 75 MG (as clopidogrel bisulfate 97.875 MG) Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Sanofi-aventis U.s. Llc
    Dosage Form:
    Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    NDA020839
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    05-09-2009
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    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.

    Frequently Asked Questions

    What is NDC 0024-1332-30?

    The NDC Packaged Code 0024-1332-30 is assigned to a package of 3 blister pack in 1 carton / 10 tablet, film coated in 1 blister pack of Plavix, a human prescription drug labeled by Sanofi-aventis U.s. Llc. The product's dosage form is tablet, film coated and is administered via oral form.

    Is NDC 0024-1332 included in the NDC Directory?

    Yes, Plavix with product code 0024-1332 is active and included in the NDC Directory. The product was first marketed by Sanofi-aventis U.s. Llc on May 09, 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 0024-1332-30?

    The 11-digit format is 00024133230. 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 4-4-2 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
    4-4-20024-1332-305-4-200024-1332-30