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  5. NDC Package Code: 64679-759-06 Furosemide

NDC Package 64679-759-06 Furosemide

Injection Intramuscular; Intravenous - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

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:
64679-759-06
Package Description:
1 VIAL, SINGLE-DOSE in 1 CARTON / 10 mL in 1 VIAL, SINGLE-DOSE (64679-759-12)
Product Code:
64679-759
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:
64679075906
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:
    Wockhardt Usa Llc.
    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):
  • FUROSEMIDE 10 mg/mL
    • Pharmacologic Class(es):
  • Increased Diuresis at Loop of Henle - [PE] (Physiologic Effect)
  • Loop Diuretic - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    ANDA077941
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    03-22-2007
    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
    64679-759-0125 VIAL, SINGLE-DOSE in 1 CARTON / 2 mL in 1 VIAL, SINGLE-DOSE (64679-759-10)
    64679-759-0225 VIAL, SINGLE-DOSE in 1 CARTON / 4 mL in 1 VIAL, SINGLE-DOSE (64679-759-11)
    64679-759-0325 VIAL, SINGLE-DOSE in 1 CARTON / 10 mL in 1 VIAL, SINGLE-DOSE (64679-759-12)
    64679-759-041 VIAL, SINGLE-DOSE in 1 CARTON / 2 mL in 1 VIAL, SINGLE-DOSE (64679-759-10)
    64679-759-051 VIAL, SINGLE-DOSE in 1 CARTON / 4 mL in 1 VIAL, SINGLE-DOSE (64679-759-11)
    64679-759-0710 VIAL, SINGLE-DOSE in 1 CARTON / 2 mL in 1 VIAL, SINGLE-DOSE (64679-759-10)
    64679-759-0810 VIAL, SINGLE-DOSE in 1 CARTON / 4 mL in 1 VIAL, SINGLE-DOSE (64679-759-11)
    64679-759-0910 VIAL, SINGLE-DOSE in 1 CARTON / 10 mL in 1 VIAL, SINGLE-DOSE (64679-759-12)

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 64679-759-06?

    The NDC Packaged Code 64679-759-06 is assigned to a package of 1 vial, single-dose in 1 carton / 10 ml in 1 vial, single-dose (64679-759-12) of Furosemide, a human prescription drug labeled by Wockhardt Usa Llc.. The product's dosage form is injection and is administered via intramuscular; intravenous form.

    Is NDC 64679-759 included in the NDC Directory?

    Yes, Furosemide with product code 64679-759 is active and included in the NDC Directory. The product was first marketed by Wockhardt Usa Llc. on March 22, 2007 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 64679-759-06?

    The 11-digit format is 64679075906. 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
    5-3-264679-759-065-4-264679-0759-06