NDC Package 51662-1482-1 Nicardipine Hydrochloride

Injection 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:
51662-1482-1
Package Description:
10 mL in 1 VIAL
Product Code:
Proprietary Name:
Nicardipine Hydrochloride
Non-Proprietary Name:
Nicardipine Hydrochloride
Substance Name:
Nicardipine Hydrochloride
Usage Information:
1.1 HypertensionNicardipine hydrochloride injection is indicated for the short-term treatment of hypertension when oral therapy is not feasible or desirable. For prolonged control of blood pressure, transfer patients to oral medication as soon as their clinical condition permits [see Dosage and Administration (2.6)].
11-Digit NDC Billing Format:
51662148201
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
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Hf Acquisition Co Llc, Dba Healthfirst
    Dosage Form:
    Injection - A sterile preparation intended for parenteral use; five distinct classes of injections exist as defined by the USP.
    Administration Route(s):
  • Intravenous - Administration within or into a vein or veins.
  • Sample Package:
    No
    FDA Application Number:
    NDA022276
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    02-01-2020
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N

    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.

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    Frequently Asked Questions

    What is NDC 51662-1482-1?

    The NDC Packaged Code 51662-1482-1 is assigned to a package of 10 ml in 1 vial of Nicardipine Hydrochloride, a human prescription drug labeled by Hf Acquisition Co Llc, Dba Healthfirst. The product's dosage form is injection and is administered via intravenous form.

    Is NDC 51662-1482 included in the NDC Directory?

    Yes, Nicardipine Hydrochloride with product code 51662-1482 is active and included in the NDC Directory. The product was first marketed by Hf Acquisition Co Llc, Dba Healthfirst on February 01, 2020 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 51662-1482-1?

    The 11-digit format is 51662148201. 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
    5-4-151662-1482-15-4-251662-1482-01