NDC Package 65862-472-30 Fosinopril Sodium

Tablet 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:
65862-472-30
Package Description:
30 TABLET in 1 BOTTLE
Product Code:
Proprietary Name:
Fosinopril Sodium
Non-Proprietary Name:
Fosinopril Sodium
Substance Name:
Fosinopril Sodium
Usage Information:
Fosinopril is used to treat high blood pressure (hypertension). Lowering high blood pressure helps prevent strokes, heart attacks, and kidney problems. It is also used to treat heart failure. Fosinopril is an ACE inhibitor and works by relaxing blood vessels so that blood can flow more easily.
11-Digit NDC Billing Format:
65862047230
NDC to RxNorm Crosswalk:
  • RxCUI: 857169 - fosinopril sodium 10 MG Oral Tablet
  • RxCUI: 857169 - FNP Sodium 10 MG Oral Tablet
  • RxCUI: 857183 - fosinopril sodium 20 MG Oral Tablet
  • RxCUI: 857183 - FNP Sodium 20 MG Oral Tablet
  • RxCUI: 857187 - fosinopril sodium 40 MG Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Aurobindo Pharma Limited
    Dosage Form:
    Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    FDA Application Number:
    ANDA091163
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    03-30-2011
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    65862-472-393000 TABLET in 1 BAG
    65862-472-9090 TABLET in 1 BOTTLE
    65862-472-991000 TABLET in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 65862-472-30?

    The NDC Packaged Code 65862-472-30 is assigned to a package of 30 tablet in 1 bottle of Fosinopril Sodium, a human prescription drug labeled by Aurobindo Pharma Limited. The product's dosage form is tablet and is administered via oral form.

    Is NDC 65862-472 included in the NDC Directory?

    Yes, Fosinopril Sodium with product code 65862-472 is active and included in the NDC Directory. The product was first marketed by Aurobindo Pharma Limited on March 30, 2011 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 65862-472-30?

    The 11-digit format is 65862047230. 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
    5-3-265862-472-305-4-265862-0472-30