NDC Package 51662-1478-3 Metoprolol Tartrate

Injection, Solution 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:
51662-1478-3
Package Description:
10 POUCH in 1 CASE / 1 VIAL, SINGLE-DOSE in 1 POUCH (51662-1478-2) / 5 mL in 1 VIAL, SINGLE-DOSE (51662-1478-1)
Product Code:
Proprietary Name:
Metoprolol Tartrate
Non-Proprietary Name:
Metoprolol Tartrate
Substance Name:
Metoprolol Tartrate
Usage Information:
Metoprolol is used with or without other medications to treat high blood pressure (hypertension). Lowering high blood pressure helps prevent strokes, heart attacks, and kidney problems. This medication is also used to treat chest pain (angina) and to improve survival after a heart attack. Metoprolol belongs to a class of drugs known as beta blockers. It works by blocking the action of certain natural chemicals in your body, such as epinephrine, on the heart and blood vessels. This effect lowers the heart rate, blood pressure, and strain on the heart.
11-Digit NDC Billing Format:
51662147803
NDC to RxNorm Crosswalk:
  • RxCUI: 866508 - metoprolol tartrate 5 MG in 5 ML Injection
  • RxCUI: 866508 - 5 ML metoprolol tartrate 1 MG/ML Injection
  • RxCUI: 866508 - metoprolol tartrate 5 MG per 5 ML Injection
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Hf Acquisition Co Llc, Dba Healthfirst
    Dosage Form:
    Injection, Solution - A liquid preparation containing one or more drug substances dissolved in a suitable solvent or mixture of mutually miscible solvents that is suitable for injection.
    Administration Route(s):
  • Intravenous - Administration within or into a vein or veins.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA078085
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    12-14-2019
    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.

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    Frequently Asked Questions

    What is NDC 51662-1478-3?

    The NDC Packaged Code 51662-1478-3 is assigned to a package of 10 pouch in 1 case / 1 vial, single-dose in 1 pouch (51662-1478-2) / 5 ml in 1 vial, single-dose (51662-1478-1) of Metoprolol Tartrate, a human prescription drug labeled by Hf Acquisition Co Llc, Dba Healthfirst. The product's dosage form is injection, solution and is administered via intravenous form.

    Is NDC 51662-1478 included in the NDC Directory?

    Yes, Metoprolol Tartrate with product code 51662-1478 is active and included in the NDC Directory. The product was first marketed by Hf Acquisition Co Llc, Dba Healthfirst on December 14, 2019 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 51662-1478-3?

    The 11-digit format is 51662147803. 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
    5-4-151662-1478-35-4-251662-1478-03