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  5. NDC Package Code: 12714-931-40 Telmisartan

NDC Package 12714-931-40 Telmisartan

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

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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.

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:
12714-931-40
Package Description:
7 mg in 1 BLISTER PACK
Product Code:
12714-931
Non-Proprietary Name:
Telmisartan
Substance Name:
Telmisartan
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.
11-Digit NDC Billing Format:
12714093140
Product Type:
Drug For Further Processing
Labeler Name:
Boehringer Ingelheim Pharma Gmbh And Co. Kg
Dosage Form:
Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
Active Ingredient(s):
TELMISARTAN 40 mg/40mg
Sample Package:
N/A
Marketing Category:
DRUG FOR FURTHER PROCESSING - A drug (other than the bulk ingredient API) that is in an interim stage of manufacture, processing, preparation, or packaging, and not ready for human or animal use.
Start Marketing Date:
12-01-2000
Listing Expiration Date:
12-31-2026
Exclude Flag:
N
Unfinished Product:
Yes
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
12714-931-4128 mg in 1 BLISTER PACK

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 12714-931-40?

The NDC Packaged Code 12714-931-40 is assigned to an UNFINISHED drug package of 7 mg in 1 blister pack of Telmisartan, drug for further processing labeled by Boehringer Ingelheim Pharma Gmbh And Co. Kg. The product's dosage form is tablet and is administered via form.

Is NDC 12714-931 included in the NDC Directory?

Yes, Telmisartan is an UNFINISHED PRODUCT with code 12714-931 that is active and included in the NDC Directory. The product was first marketed by Boehringer Ingelheim Pharma Gmbh And Co. Kg on December 01, 2000 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 12714-931-40?

The 11-digit format is 12714093140. 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
5-3-212714-931-405-4-212714-0931-40