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  5. NDC Package Code: 70771-1106-1 Ethacrynate Sodium

NDC Package 70771-1106-1 Ethacrynate Sodium

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

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:
70771-1106-1
Package Description:
1 VIAL in 1 CARTON / 50 mL in 1 VIAL
Product Code:
70771-1106
Proprietary Name:
Ethacrynate Sodium
Usage Information:
Ethacrynic acid is indicated for treatment of edema when an agent with greater diuretic potential than those commonly employed is required.Treatment of the edema associated with congestive heart failure, cirrhosis of the liver, and renal disease, including the nephrotic syndrome.Short-term management of ascites due to malignancy, idiopathic edema, and lymphedema.Short-term management of hospitalized pediatric patients, other than infants, with congenital heart disease or the nephrotic syndrome.Intravenous ETHACRYNATE SODIUM FOR INJECTION, USP is indicated when a rapid onset of diuresis is desired, e.g., in acute pulmonary edema, or when gastrointestinal absorption is impaired or oral medication is not practicable.
11-Digit NDC Billing Format:
70771110601
Labeler Name:
Zydus Lifesciences Limited
Sample Package:
No
FDA Application Number:
ANDA207758
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
01-24-2018
End Marketing Date:
06-03-2025
Listing Expiration Date:
06-03-2025
Exclude Flag:
D
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 70771-1106-1?

The NDC Packaged Code 70771-1106-1 is assigned to a package of 1 vial in 1 carton / 50 ml in 1 vial of Ethacrynate Sodium, labeled by Zydus Lifesciences Limited. The product's dosage form is and is administered via form.

Is NDC 70771-1106 included in the NDC Directory?

No, Ethacrynate Sodium with product code 70771-1106 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Zydus Lifesciences Limited on January 24, 2018 and its listing in the NDC Directory is set to expire on June 03, 2025 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 70771-1106-1?

The 11-digit format is 70771110601. 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 5-4-1 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
5-4-170771-1106-15-4-270771-1106-01