NDC Package 0597-0039-37 Micardis

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

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:
0597-0039-37
Package Description:
3 BLISTER PACK in 1 CARTON / 10 TABLET in 1 BLISTER PACK
Product Code:
Proprietary Name:
Micardis
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:
00597003937
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
3 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 205304 - telmisartan 40 MG Oral Tablet
  • RxCUI: 205305 - telmisartan 80 MG Oral Tablet
  • RxCUI: 213431 - Micardis 40 MG Oral Tablet
  • RxCUI: 213431 - telmisartan 40 MG Oral Tablet [Micardis]
  • RxCUI: 213432 - Micardis 80 MG Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Boehringer Ingelheim Pharmaceuticals, 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):
    Sample Package:
    No
    FDA Application Number:
    NDA020850
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    12-01-2000
    End Marketing Date:
    04-30-2025
    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 0597-0039-37?

    The NDC Packaged Code 0597-0039-37 is assigned to a package of 3 blister pack in 1 carton / 10 tablet in 1 blister pack of Micardis, a human prescription drug labeled by Boehringer Ingelheim Pharmaceuticals, Inc.. The product's dosage form is tablet and is administered via oral form.

    Is NDC 0597-0039 included in the NDC Directory?

    Yes, Micardis with product code 0597-0039 is active and included in the NDC Directory. The product was first marketed by Boehringer Ingelheim Pharmaceuticals, Inc. on December 01, 2000.

    What is the NDC billing unit for package 0597-0039-37?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 3.

    What is the 11-digit format for NDC 0597-0039-37?

    The 11-digit format is 00597003937. 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
    4-4-20597-0039-375-4-200597-0039-37