Telmisartan Powder
NDC Package 12666-0010-1

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

Package Information

This product is an UNFINISHED DRUG part of the official NDC directory. Unfinished drugs include products like active ingredients some of which are used in bulk for further processing or compounding. The FDA requires a list of these drugs manufactured in a U.S. commercial distribution facility.

Telmisartan powders is a medication used to treat high blood pressure (hypertension). This formulation utilizes a powder delivery system. Marketed by Zhejiang Apeloa Jiayuan Pharmaceutical Co., Ltd., this product is identified by NDC 12666-0010.

Identification & Billing

NDC Package Code
12666-0010-1
Package Description
25 kg in 1 DRUM
Product Code
12666-0010
11-Digit Billing Format
12666001001

Clinical Specifications

Proprietary Name
Telmisartan
Non-Proprietary Name
Telmisartan
Substance Name
Telmisartan
Dosage Form
Powder - An intimate mixture of dry, finely divided drugs and/or chemicals that may be intended for internal or external use.
Active Ingredient(s)
TELMISARTAN 1 kg/kg
Usage Information
This medication is used to treat high blood pressure (hypertension). Lowering high blood pressure helps prevent strokes, heart attacks, and kidney problems. Telmisartan belongs to a class of drugs called angiotensin receptor blockers (ARBs). It works by relaxing blood vessels so blood can flow more easily.

Regulatory & Marketing

Labeler Name
Zhejiang Apeloa Jiayuan Pharmaceutical Co., Ltd.
Product Type
Bulk Ingredient
Marketing Category
BULK INGREDIENT - A category specifying that a product is marketed as a bulk ingredient.
Start Marketing Date
12-10-2009
Listing Expiration
12-31-2026
Exclude Flag
N
Unfinished Product
Yes
Sample Package
N/A

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 12666-0010-1 identifies a specific commercial package of 25 kg in 1 drum of Telmisartan (UNFINISHED drug), a bulk ingredient labeled by Zhejiang Apeloa Jiayuan Pharmaceutical Co., Ltd.. This powder is formulated for use and contains telmisartan 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 Zhejiang Apeloa Jiayuan Pharmaceutical Co., Ltd. on December 10, 2009. The current certification is valid through December 31, 2026.

What are the primary indications for this medication?

This medication is used to treat high blood pressure (hypertension). Lowering high blood pressure helps prevent strokes, heart attacks, and kidney problems. Telmisartan belongs to a class of drugs called angiotensin receptor blockers (ARBs). It works by relaxing blood vessels so blood can flow more easily.

How is this Zhejiang Apeloa Jiayuan Pharmaceutical Co., Ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 12666001001. 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 (5-4-1)
12666-0010-1
11-Digit CMS (5-4-2)
12666-0010-01

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