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  5. NDC Package Code: 60468-001-01 Bumetanide

NDC Package 60468-001-01 Bumetanide

Tablet - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

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:
60468-001-01
Package Description:
80000 TABLET in 1 CONTAINER
Product Code:
60468-001
Non-Proprietary Name:
Bumetanide
Substance Name:
Bumetanide
Usage Information:
Bumetanide is used to reduce extra fluid in the body (edema) caused by conditions such as heart failure, liver disease, and kidney disease. This can lessen symptoms such as shortness of breath and swelling in your arms, legs, and abdomen. Bumetanide is a "water pill" (diuretic) that causes you to make more urine. This helps your body get rid of extra water and salt.
11-Digit NDC Billing Format:
60468000101
Product Type:
Bulk Ingredient
Labeler Name:
Allphamed Pharbil Arzneimittel Gmbh
Dosage Form:
Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
Active Ingredient(s):
  • BUMETANIDE .5 mg/1
    • Sample Package:
    N/A
    Marketing Category:
    DRUG FOR FURTHER PROCESSING - A drug (other than the bulk ingredient API) that is in an interim stage of manufacture, processing, preparation, or packaging, and not ready for human or animal use.
    Start Marketing Date:
    08-10-2015
    Listing Expiration Date:
    12-31-2024
    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.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 60468-001-01?

    The NDC Packaged Code 60468-001-01 is assigned to an UNFINISHED drug package of 80000 tablet in 1 container of Bumetanide, a bulk ingredient labeled by Allphamed Pharbil Arzneimittel Gmbh. The product's dosage form is tablet and is administered via form.

    Is NDC 60468-001 included in the NDC Directory?

    Yes, Bumetanide is an UNFINISHED PRODUCT with code 60468-001 that is active and included in the NDC Directory. The product was first marketed by Allphamed Pharbil Arzneimittel Gmbh on August 10, 2015 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 60468-001-01?

    The 11-digit format is 60468000101. 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
    5-3-260468-001-015-4-260468-0001-01