NDC Package 50228-111-30 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:
50228-111-30
Package Description:
30 TABLET in 1 BOTTLE
Product Code:
Proprietary Name:
Hydrochlorothiazide
Non-Proprietary Name:
Hydrochlorothiazide
Substance Name:
Hydrochlorothiazide
Usage Information:
This medication is used to treat high blood pressure. Lowering high blood pressure helps prevent strokes, heart attacks, and kidney problems. Hydrochlorothiazide belongs to a class of drugs known as diuretics/"water pills." It works by causing you to make more urine. This helps your body get rid of extra salt and water. This medication also reduces extra fluid in the body (edema) caused by conditions such as heart failure, liver disease, or kidney disease. This can lessen symptoms such as shortness of breath or swelling in your ankles or feet.
11-Digit NDC Billing Format:
50228011130
NDC to RxNorm Crosswalk:
  • RxCUI: 197770 - hydroCHLOROthiazide 50 MG Oral Tablet
  • RxCUI: 197770 - hydrochlorothiazide 50 MG Oral Tablet
  • RxCUI: 197770 - HCTZ 50 MG Oral Tablet
  • RxCUI: 310798 - hydroCHLOROthiazide 25 MG Oral Tablet
  • RxCUI: 310798 - hydrochlorothiazide 25 MG Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Sciegen Pharmaceuticals, 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):
    Sample Package:
    No
    FDA Application Number:
    ANDA203018
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    07-23-2014
    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
    50228-111-101000 TABLET in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 50228-111-30?

    The NDC Packaged Code 50228-111-30 is assigned to a package of 30 tablet in 1 bottle of Hydrochlorothiazide, a human prescription drug labeled by Sciegen Pharmaceuticals, Inc.. The product's dosage form is tablet and is administered via oral form.

    Is NDC 50228-111 included in the NDC Directory?

    Yes, Hydrochlorothiazide with product code 50228-111 is active and included in the NDC Directory. The product was first marketed by Sciegen Pharmaceuticals, Inc. on July 23, 2014 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 50228-111-30?

    The 11-digit format is 50228011130. 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
    5-3-250228-111-305-4-250228-0111-30