NDC Package 30698-461-01 Lopressor Hct

Metoprolol Tartrate And Hydrochlorothiazide Tablet 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:
30698-461-01
Package Description:
100 TABLET in 1 BOTTLE
Product Code:
Proprietary Name:
Lopressor Hct
Non-Proprietary Name:
Metoprolol Tartrate And Hydrochlorothiazide
Substance Name:
Hydrochlorothiazide; Metoprolol Tartrate
Usage Information:
Lopressor HCT is indicated for the management of hypertension.This fixed-combination drug is not indicated for initial therapy of hypertension. If the fixed combination represents the dose titrated to the individual patient's needs, therapy with the fixed combination may be more convenient than with the separate components.
11-Digit NDC Billing Format:
30698046101
NDC to RxNorm Crosswalk:
  • RxCUI: 866479 - metoprolol tartrate 100 MG / hydroCHLOROthiazide 25 MG Oral Tablet
  • RxCUI: 866479 - hydrochlorothiazide 25 MG / metoprolol tartrate 100 MG Oral Tablet
  • RxCUI: 866479 - HCTZ 25 MG / metoprolol tartrate 100 MG Oral Tablet
  • RxCUI: 866482 - metoprolol tartrate 50 MG / hydroCHLOROthiazide 25 MG Oral Tablet
  • RxCUI: 866482 - hydrochlorothiazide 25 MG / metoprolol tartrate 50 MG Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Validus Pharmaceuticals Llc
    Dosage Form:
    Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    FDA Application Number:
    NDA018303
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    06-30-2014
    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 30698-461-01?

    The NDC Packaged Code 30698-461-01 is assigned to a package of 100 tablet in 1 bottle of Lopressor Hct, a human prescription drug labeled by Validus Pharmaceuticals Llc. The product's dosage form is tablet and is administered via oral form.

    Is NDC 30698-461 included in the NDC Directory?

    Yes, Lopressor Hct with product code 30698-461 is active and included in the NDC Directory. The product was first marketed by Validus Pharmaceuticals Llc on June 30, 2014 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 30698-461-01?

    The 11-digit format is 30698046101. 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
    5-3-230698-461-015-4-230698-0461-01