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  5. NDC Package Code: 51672-4046-3 Enalapril Maleate And Hydrochlorothiazide

NDC Package 51672-4046-3 Enalapril Maleate And Hydrochlorothiazide

Tablet Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
51672-4046-3
Package Description:
1000 TABLET in 1 BOTTLE
Product Code:
51672-4046
Proprietary Name:
Enalapril Maleate And Hydrochlorothiazide
Non-Proprietary Name:
Enalapril Maleate And Hydrochlorothiazide
Substance Name:
Enalapril Maleate; Hydrochlorothiazide
Usage Information:
Enalapril maleate and hydrochlorothiazide is indicated for the treatment of hypertension.This fixed dose combination is not indicated for initial treatment (see DOSAGE AND ADMINISTRATION).In using enalapril maleate and hydrochlorothiazide, consideration should be given to the fact that another angiotensin converting enzyme inhibitor, captopril, has caused agranulocytosis, particularly in patients with renal impairment or collagen vascular disease, and that available data are insufficient to show that enalapril does not have a similar risk (see WARNINGS).In considering use of enalapril maleate and hydrochlorothiazide, it should be noted that black patients receiving ACE inhibitors have been reported to have a higher incidence of angioedema compared to non-blacks (see WARNINGS, Head and Neck Angioedema).
11-Digit NDC Billing Format:
51672404603
NDC to RxNorm Crosswalk:
  • RxCUI: 858824 - enalapril maleate 5 MG / hydroCHLOROthiazide 12.5 MG Oral Tablet
  • RxCUI: 858824 - enalapril maleate 5 MG / hydrochlorothiazide 12.5 MG Oral Tablet
  • RxCUI: 858824 - enalapril maleate 5 MG / HCTZ 12.5 MG Oral Tablet
  • RxCUI: 858828 - enalapril maleate 10 MG / hydroCHLOROthiazide 25 MG Oral Tablet
  • RxCUI: 858828 - enalapril maleate 10 MG / hydrochlorothiazide 25 MG Oral Tablet
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Taro Pharmaceuticals U.s.a., Inc.
    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.
    • Active Ingredient(s):
  • ENALAPRIL MALEATE 10 mg/1
  • HYDROCHLOROTHIAZIDE 25 mg/1
    • Pharmacologic Class(es):
  • Angiotensin Converting Enzyme Inhibitor - [EPC] (Established Pharmacologic Class)
  • Angiotensin-converting Enzyme Inhibitors - [MoA] (Mechanism of Action)
  • Decreased Blood Pressure - [PE] (Physiologic Effect)
  • Increased Diuresis - [PE] (Physiologic Effect)
  • Thiazide Diuretic - [EPC] (Established Pharmacologic Class)
  • Thiazides - [CS]
    • Sample Package:
    No
    FDA Application Number:
    ANDA075788
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    09-18-2001
    End Marketing Date:
    01-01-2025
    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.

    * Please review the disclaimer below.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    51672-4046-1100 TABLET in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 51672-4046-3?

    The NDC Packaged Code 51672-4046-3 is assigned to a package of 1000 tablet in 1 bottle of Enalapril Maleate And Hydrochlorothiazide, a human prescription drug labeled by Taro Pharmaceuticals U.s.a., Inc.. The product's dosage form is tablet and is administered via oral form.

    Is NDC 51672-4046 included in the NDC Directory?

    Yes, Enalapril Maleate And Hydrochlorothiazide with product code 51672-4046 is active and included in the NDC Directory. The product was first marketed by Taro Pharmaceuticals U.s.a., Inc. on September 18, 2001.

    What is the 11-digit format for NDC 51672-4046-3?

    The 11-digit format is 51672404603. 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
    5-4-151672-4046-35-4-251672-4046-03