NDC Package 71610-565-45 Metoprolol Tartrate

Tablet, Film Coated Oral - 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:
71610-565-45
Package Description:
45 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
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:
71610056545
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
45 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 866511 - metoprolol tartrate 100 MG Oral Tablet
  • RxCUI: 866514 - metoprolol tartrate 50 MG Oral Tablet
  • RxCUI: 866924 - metoprolol tartrate 25 MG Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Aphena Pharma Solutions - Tennessee, Llc
    Dosage Form:
    Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA076704
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    01-16-2004
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    71610-565-3030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
    71610-565-5360 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
    71610-565-6090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
    71610-565-70120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
    71610-565-73135 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
    71610-565-80180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
    71610-565-92270 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
    71610-565-94360 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
    71610-565-98540 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 71610-565-45?

    The NDC Packaged Code 71610-565-45 is assigned to a package of 45 tablet, film coated in 1 bottle, plastic of Metoprolol Tartrate, a human prescription drug labeled by Aphena Pharma Solutions - Tennessee, Llc. The product's dosage form is tablet, film coated and is administered via oral form.This product is billed for "EA" each discreet unit and contains an estimated amount of 45 billable units per package.

    Is NDC 71610-565 included in the NDC Directory?

    Yes, Metoprolol Tartrate with product code 71610-565 is active and included in the NDC Directory. The product was first marketed by Aphena Pharma Solutions - Tennessee, Llc on January 16, 2004 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 NDC billing unit for package 71610-565-45?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 45.

    What is the 11-digit format for NDC 71610-565-45?

    The 11-digit format is 71610056545. 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 5-3-2 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
    5-3-271610-565-455-4-271610-0565-45