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  5. NDC Package Code: 70710-1785-6 Norepinephrine Bitartrate

NDC Package 70710-1785-6 Norepinephrine Bitartrate

Injection, Solution, Concentrate Intravenous - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. 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:
70710-1785-6
Package Description:
10 VIAL, GLASS in 1 CARTON / 4 mL in 1 VIAL, GLASS (70710-1785-1)
Product Code:
70710-1785
Proprietary Name:
Norepinephrine Bitartrate
Non-Proprietary Name:
Norepinephrine Bitartrate
Substance Name:
Norepinephrine Bitartrate
Usage Information:
Norepinephrine bitartrate injection is indicated to raise blood pressure in adult patients with severe, acute hypotension.
11-Digit NDC Billing Format:
70710178506
NDC to RxNorm Crosswalk:
Product Type:
Human Prescription Drug
Labeler Name:
Zydus Pharmaceuticals Usa Inc.
Dosage Form:
Injection, Solution, Concentrate - A sterile preparation for parenteral use which, upon the addition of suitable solvents, yields a solution conforming in all respects to the requirements for Injections.
Administration Route(s):
Intravenous - Administration within or into a vein or veins.
Active Ingredient(s):
NOREPINEPHRINE BITARTRATE 1 mg/mL
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
ANDA216341
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
04-24-2024
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 70710-1785-6?

The NDC Packaged Code 70710-1785-6 is assigned to a package of 10 vial, glass in 1 carton / 4 ml in 1 vial, glass (70710-1785-1) of Norepinephrine Bitartrate, a human prescription drug labeled by Zydus Pharmaceuticals Usa Inc.. The product's dosage form is injection, solution, concentrate and is administered via intravenous form.

Is NDC 70710-1785 included in the NDC Directory?

Yes, Norepinephrine Bitartrate with product code 70710-1785 is active and included in the NDC Directory. The product was first marketed by Zydus Pharmaceuticals Usa Inc. on April 24, 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 70710-1785-6?

The 11-digit format is 70710178506. 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
5-4-170710-1785-65-4-270710-1785-06