Olmesartan Medoxomil And Hydrochlorothiazide Tablet
NDC Package 62332-151-91

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

Olmesartan Medoxomil And Hydrochlorothiazide tablets are indicated for the treatment of hypertension, to lower blood pressure. This formulation utilizes a tablet delivery system. Marketed by Alembic Pharmaceuticals Inc., this product is identified by NDC 62332-151 and is authorized under FDA application ANDA204233.

Identification & Billing

NDC Package Code
62332-151-91
Package Description
1000 TABLET in 1 BOTTLE
Product Code
11-Digit Billing Format
62332015191
RxNorm Crosswalk
  • RxCUI: 403853 - olmesartan medoxomil 20 MG / hydroCHLOROthiazide 12.5 MG Oral Tablet
  • RxCUI: 403853 - hydrochlorothiazide 12.5 MG / olmesartan medoxomil 20 MG Oral Tablet
  • RxCUI: 403853 - HCTZ 12.5 MG / olmesartan medoxomil 20 MG Oral Tablet
  • RxCUI: 403854 - olmesartan medoxomil 40 MG / hydroCHLOROthiazide 12.5 MG Oral Tablet
  • RxCUI: 403854 - hydrochlorothiazide 12.5 MG / olmesartan medoxomil 40 MG Oral Tablet

Clinical Specifications

Proprietary Name
Olmesartan Medoxomil And Hydrochlorothiazide
Non-Proprietary Name
Olmesartan Medoxomil And Hydrochlorothiazide
Substance Name
Hydrochlorothiazide; Olmesartan Medoxomil
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.
Usage Information
Olmesartan medoxomil and hydrochlorothiazide tablets are indicated for the treatment of hypertension, to lower blood pressure. Olmesartan medoxomil and hydrochlorothiazide tablets are not indicated for the initial therapy of hypertension [see Dosage and Administration (2)]. Lowering blood pressure reduces the risk of fatal and nonfatal 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 the class to which this drug principally belongs. There are no controlled trials demonstrating risk reduction with olmesartan medoxomil and hydrochlorothiazide tablets. 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 one 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 (e.g., on angina, heart failure, or diabetic kidney disease). These considerations may guide selection of therapy. Olmesartan medoxomil and hydrochlorothiazide tablets may be used alone, or in combination with other antihypertensive drugs.

Regulatory & Marketing

Labeler Name
Alembic Pharmaceuticals Inc.
Product Type
Human Prescription Drug
FDA Application #
ANDA204233
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
04-24-2017
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy 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 full disclaimer at the bottom of this page.

Other Available Packages

The following commercial packages are registered under the same Product NDC (62332-151). Click a package code to view its specific billing and regulatory data.

80 TABLET in 1 CARTON
100 TABLET in 1 CARTON
30 TABLET in 1 BOTTLE
90 TABLET in 1 BOTTLE

* 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 62332-151-91 identifies a specific commercial package of 1000 tablet in 1 bottle of Olmesartan Medoxomil And Hydrochlorothiazide, a human prescription drug labeled by Alembic Pharmaceuticals Inc.. This tablet is formulated for oral use and contains hydrochlorothiazide; olmesartan medoxomil 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 Alembic Pharmaceuticals Inc. on April 24, 2017. The current certification is valid through December 31, 2026.

How is this Alembic Pharmaceuticals Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 62332015191. 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)
62332-151-91
11-Digit CMS (5-4-2)
62332-0151-91

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