NDC Package 0143-9155-25 Furosemide

Injection Intramuscular; Intravenous - 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:
0143-9155-25
Package Description:
25 VIAL, SINGLE-DOSE in 1 CARTON / 2 mL in 1 VIAL, SINGLE-DOSE (0143-9155-01)
Product Code:
Proprietary Name:
Furosemide
Non-Proprietary Name:
Furosemide
Substance Name:
Furosemide
Usage Information:
Furosemide 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. This drug is also used to treat high blood pressure. Lowering high blood pressure helps prevent strokes, heart attacks, and kidney problems. Furosemide 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:
00143915525
NDC to RxNorm Crosswalk:
  • RxCUI: 1719286 - furosemide 100 MG in 10 ML Injection
  • RxCUI: 1719286 - 10 ML furosemide 10 MG/ML Injection
  • RxCUI: 1719286 - furosemide 100 MG per 10 ML Injection
  • RxCUI: 1719290 - furosemide 20 MG in 2 ML Injection
  • RxCUI: 1719290 - 2 ML furosemide 10 MG/ML Injection
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Hikma Pharmaceuticals Usa Inc.
    Dosage Form:
    Injection - A sterile preparation intended for parenteral use; five distinct classes of injections exist as defined by the USP.
    Administration Route(s):
  • Intramuscular - Administration within a muscle.
  • Intravenous - Administration within or into a vein or veins.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    NDA018267
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    05-31-2024
    Listing Expiration Date:
    12-31-2025
    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 0143-9155-25?

    The NDC Packaged Code 0143-9155-25 is assigned to a package of 25 vial, single-dose in 1 carton / 2 ml in 1 vial, single-dose (0143-9155-01) of Furosemide, a human prescription drug labeled by Hikma Pharmaceuticals Usa Inc.. The product's dosage form is injection and is administered via intramuscular; intravenous form.

    Is NDC 0143-9155 included in the NDC Directory?

    Yes, Furosemide with product code 0143-9155 is active and included in the NDC Directory. The product was first marketed by Hikma Pharmaceuticals Usa Inc. on May 31, 2024 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 0143-9155-25?

    The 11-digit format is 00143915525. 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
    4-4-20143-9155-255-4-200143-9155-25