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  5. NDC Package Code: 51662-1475-1 Vecuronium Bromide

NDC Package 51662-1475-1 Vecuronium Bromide

Injection, Powder, Lyophilized, For Solution 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:
51662-1475-1
Package Description:
10 mL in 1 VIAL
Product Code:
51662-1475
Proprietary Name:
Vecuronium Bromide
Non-Proprietary Name:
Vecuronium Bromide
Substance Name:
Vecuronium Bromide
Usage Information:
Vecuronium bromide is indicated as an adjunct to general anesthesia, to facilitate endotracheal intubation and to provide skeletal muscle relaxation during surgery or mechanical ventilation.
11-Digit NDC Billing Format:
51662147501
NDC to RxNorm Crosswalk:
  • RxCUI: 859437 - vecuronium bromide 1 MG/ML Injectable Solution
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Hf Acquisition Co Llc, Dba Healthfirst
    Dosage Form:
    Injection, Powder, Lyophilized, For Solution - A dosage form intended for the solution prepared by lyophilization ("freeze drying"), a process which involves the removal of water from products in the frozen state at extremely low pressures; this is intended for subsequent addition of liquid to create a solution that conforms in all respects to the requirements for Injections.
    Administration Route(s):
  • Intravenous - Administration within or into a vein or veins.
    • Active Ingredient(s):
  • VECURONIUM BROMIDE 1 mg/mL
    • Pharmacologic Class(es):
  • Neuromuscular Nondepolarizing Blockade - [PE] (Physiologic Effect)
  • Nondepolarizing Neuromuscular Blocker - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    ANDA075164
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    12-15-2019
    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.

    Frequently Asked Questions

    What is NDC 51662-1475-1?

    The NDC Packaged Code 51662-1475-1 is assigned to a package of 10 ml in 1 vial of Vecuronium Bromide, a human prescription drug labeled by Hf Acquisition Co Llc, Dba Healthfirst. The product's dosage form is injection, powder, lyophilized, for solution and is administered via intravenous form.

    Is NDC 51662-1475 included in the NDC Directory?

    Yes, Vecuronium Bromide with product code 51662-1475 is active and included in the NDC Directory. The product was first marketed by Hf Acquisition Co Llc, Dba Healthfirst on December 15, 2019 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 51662-1475-1?

    The 11-digit format is 51662147501. 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
    5-4-151662-1475-15-4-251662-1475-01