NDC Package 0185-0130-05 Bumetanide

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:
0185-0130-05
Package Description:
500 TABLET in 1 BOTTLE
Product Code:
Proprietary Name:
Bumetanide
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:
00185013005
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
500 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 197417 - bumetanide 0.5 MG Oral Tablet
  • RxCUI: 197418 - bumetanide 1 MG Oral Tablet
  • RxCUI: 197419 - bumetanide 2 MG Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Eon Labs, Inc.
    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.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA074700
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    11-21-1996
    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
    0185-0130-01100 TABLET in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 0185-0130-05?

    The NDC Packaged Code 0185-0130-05 is assigned to a package of 500 tablet in 1 bottle of Bumetanide, a human prescription drug labeled by Eon Labs, Inc.. The product's dosage form is tablet and is administered via oral form.

    Is NDC 0185-0130 included in the NDC Directory?

    Yes, Bumetanide with product code 0185-0130 is active and included in the NDC Directory. The product was first marketed by Eon Labs, Inc. on November 21, 1996 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 NDC billing unit for package 0185-0130-05?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 500.

    What is the 11-digit format for NDC 0185-0130-05?

    The 11-digit format is 00185013005. 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
    4-4-20185-0130-055-4-200185-0130-05