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  5. NDC Package Code: 0781-3204-95 Nicardipine Hydrochloride

NDC Package 0781-3204-95 Nicardipine Hydrochloride

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 inactivated by the FDA.

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:
0781-3204-95
Package Description:
10 CARTON in 1 CARTON / 1 VIAL, SINGLE-DOSE in 1 CARTON (0781-3204-70) / 10 mL in 1 VIAL, SINGLE-DOSE
Product Code:
0781-3204
Proprietary Name:
Nicardipine Hydrochloride
Usage Information:
Nicardipine hydrochloride injection is indicated for the short-term treatment of hypertension when oral therapy is not feasible or not desirable. For prolonged control of blood pressure, transfer patients to oral medication as soon as their clinical condition permits (see “ DOSAGE AND ADMINISTRATION”).
11-Digit NDC Billing Format:
00781320495
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 858607 - niCARdipine HCl 25 MG in 10 ML Injection
  • RxCUI: 858607 - 10 ML nicardipine hydrochloride 2.5 MG/ML Injection
  • RxCUI: 858607 - nicardipine hydrochloride 25 MG per 10 ML Injection
    • Labeler Name:
    Sandoz Inc.
    Sample Package:
    No
    Start Marketing Date:
    11-17-2009
    Listing Expiration Date:
    12-31-2017
    Exclude Flag:
    I
    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 0781-3204-95?

    The NDC Packaged Code 0781-3204-95 is assigned to a package of 10 carton in 1 carton / 1 vial, single-dose in 1 carton (0781-3204-70) / 10 ml in 1 vial, single-dose of Nicardipine Hydrochloride, labeled by Sandoz Inc.. The product's dosage form is and is administered via form.

    Is NDC 0781-3204 included in the NDC Directory?

    No, Nicardipine Hydrochloride with product code 0781-3204 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Sandoz Inc. on November 17, 2009 and its listing in the NDC Directory is set to expire on December 31, 2017 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 0781-3204-95?

    The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.

    What is the 11-digit format for NDC 0781-3204-95?

    The 11-digit format is 00781320495. 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
    4-4-20781-3204-955-4-200781-3204-95