Metoprolol Tartrate And Hydrochlorothiazide Tablet
NDC Package 27241-301-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Metoprolol Tartrate And Hydrochlorothiazide tablets is indicated for the treatment of hypertension, to lower blood pressure. This formulation utilizes a tablet delivery system. Marketed by Ajanta Pharma Usa Inc., this product is identified by NDC 27241-301 and is authorized under FDA application ANDA215789.

Identification & Billing

NDC Package Code
27241-301-01
Package Description
100 TABLET in 1 BOTTLE
Product Code
27241-301
11-Digit Billing Format
27241030101
Billing Unit
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
Units Per Package
100 EA
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

Clinical Specifications

Proprietary Name
Metoprolol Tartrate And Hydrochlorothiazide
Non-Proprietary Name
Metoprolol Tartrate And Hydrochlorothiazide
Substance Name
Hydrochlorothiazide; Metoprolol Tartrate
Dosage Form
Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
Metoprolol tartrate and hydrochlorothiazide tablets is indicated for the treatment of hypertension, to lower blood pressure. Lowering blood pressure lowers the risk of fatal and non-fatal cardiovascular events, primarily strokes and myocardial infarctions. These benefits have been seen in controlled trials of antihypertensive drugs from a wide variety of pharmacologic classes including metoprolol.Control of high blood pressure should be part of comprehensive cardiovascular risk management, including, as appropriate, lipid control, diabetes management, antithrombotic therapy, smoking cessation, exercise, and limited sodium intake. Many patients will require more than 1 drug to achieve blood pressure goals. For specific advice on goals and management, see published guidelines, such as those of the National High Blood Pressure Education Program's Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure (JNC).Numerous antihypertensive drugs, from a variety of pharmacologic classes and with different mechanisms of action, have been shown in randomized controlled trials to reduce cardiovascular morbidity and mortality, and it can be concluded that it is blood pressure reduction, and not some other pharmacologic property of the drugs, that is largely responsible for those benefits. The largest and most consistent cardiovascular outcome benefit has been a reduction in the risk of stroke, but reductions in myocardial infarction and cardiovascular mortality also have been seen regularly.Elevated systolic or diastolic pressure causes increased cardiovascular risk, and the absolute risk increase per mmHg is greater at higher blood pressures, so that even modest reductions of severe hypertension can provide substantial benefit. Relative risk reduction from blood pressure reduction is similar across populations with varying absolute risk, so the absolute benefit is greater in patients who are at higher risk independent of their hypertension (for example, patients with diabetes or hyperlipidemia), and such patients would be expected to benefit from more aggressive treatment to a lower blood pressure goal.Some antihypertensive drugs have smaller blood pressure effects (as monotherapy) in black patients, and many antihypertensive drugs have additional approved indications and effects (eg, on angina, heart failure, or diabetic kidney disease). These considerations may guide selection of therapy.Metoprolol tartrate and hydrochlorothiazide tablets may be administered with other antihypertensive agents. Limitation of UseMetoprolol tartrate and hydrochlorothiazide tablets 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.

Regulatory & Marketing

Labeler Name
Ajanta Pharma Usa Inc.
Product Type
Human Prescription Drug
FDA Application #
ANDA215789
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
03-15-2025
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 27241-301-01 identifies a specific commercial package of 100 tablet in 1 bottle of Metoprolol Tartrate And Hydrochlorothiazide, a human prescription drug labeled by Ajanta Pharma Usa Inc.. This tablet is formulated for oral use and contains hydrochlorothiazide; metoprolol tartrate as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Ajanta Pharma Usa Inc. on March 15, 2025. The current certification is valid through December 31, 2026.

How is this Ajanta Pharma Usa Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 27241030101. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 100 total billable units per package. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
27241-301-01
11-Digit CMS (5-4-2)
27241-0301-01

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.