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  5. NDC Package Code: 0172-3444-80 Hydrochlorothiazide

NDC Package 0172-3444-80 Hydrochlorothiazide

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

Table of Contents

    1. Package Information
    2. 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:
0172-3444-80
Package Description:
1000 TABLET in 1 BOTTLE
Product Code:
0172-3444
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:
00172344480
NDC to RxNorm Crosswalk:
Product Type:
Human Prescription Drug
Labeler Name:
Teva Pharmaceuticals Usa, 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):
HYDROCHLOROTHIAZIDE 12.5 mg/1
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
ANDA083177
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
06-03-2025
Listing Expiration Date:
12-31-2026
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.

Frequently Asked Questions

What is NDC 0172-3444-80?

The NDC Packaged Code 0172-3444-80 is assigned to a package of 1000 tablet in 1 bottle of Hydrochlorothiazide, a human prescription drug labeled by Teva Pharmaceuticals Usa, Inc.. The product's dosage form is tablet and is administered via oral form.

Is NDC 0172-3444 included in the NDC Directory?

Yes, Hydrochlorothiazide with product code 0172-3444 is active and included in the NDC Directory. The product was first marketed by Teva Pharmaceuticals Usa, Inc. on June 03, 2025 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 0172-3444-80?

The 11-digit format is 00172344480. 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 4-4-2 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
4-4-20172-3444-805-4-200172-3444-80