NDC Package 68462-295-90 Trandolapril And Verapamil Hydrochloride

Tablet, Film Coated, Extended Release 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:
68462-295-90
Package Description:
90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
Product Code:
Proprietary Name:
Trandolapril And Verapamil Hydrochloride
Non-Proprietary Name:
Trandolapril And Verapamil Hydrochloride
Substance Name:
Trandolapril; Verapamil Hydrochloride
Usage Information:
Trandolapril and verapamil hydrochloride extended-release tablets are indicated for the treatment of hypertension.This fixed combination drug is not indicated for the initial therapy of hypertension (see DOSAGE AND ADMINISTRATION).In using trandolapril and verapamil hydrochloride extended-release tablets, consideration should be given to the fact that an angiotensin converting enzyme inhibitor, captopril, has caused agranulocytosis, particularly in patients with renal impairment or collagen vascular disease, and that available data are insufficient to show that trandolapril does not have similar risk (see WARNINGS - Neutropenia/Agranulocytosis).
11-Digit NDC Billing Format:
68462029590
NDC to RxNorm Crosswalk:
  • RxCUI: 897781 - trandolapril 1 MG / verapamil HCl 240 MG 24HR Extended Release Oral Tablet
  • RxCUI: 897781 - 24 HR trandolapril 1 MG / verapamil hydrochloride 240 MG Extended Release Oral Tablet
  • RxCUI: 897781 - trandolapril 1 MG / verapamil hydrochloride 240 MG 24 HR Extended Release Oral Tablet
  • RxCUI: 897783 - trandolapril 2 MG / verapamil HCl 180 MG 24HR Extended Release Oral Tablet
  • RxCUI: 897783 - 24 HR trandolapril 2 MG / verapamil hydrochloride 180 MG Extended Release Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Glenmark Pharmaceuticals Inc., Usa
    Dosage Form:
    Tablet, Film Coated, Extended Release - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer; the tablet is formulated in such manner as to make the contained medicament available over an extended period of time following ingestion.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    FDA Application Number:
    ANDA079135
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    02-25-2015
    Listing Expiration Date:
    12-31-2025
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    68462-295-01100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
    68462-295-101000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 68462-295-90?

    The NDC Packaged Code 68462-295-90 is assigned to a package of 90 tablet, film coated, extended release in 1 bottle of Trandolapril And Verapamil Hydrochloride, a human prescription drug labeled by Glenmark Pharmaceuticals Inc., Usa. The product's dosage form is tablet, film coated, extended release and is administered via oral form.

    Is NDC 68462-295 included in the NDC Directory?

    Yes, Trandolapril And Verapamil Hydrochloride with product code 68462-295 is active and included in the NDC Directory. The product was first marketed by Glenmark Pharmaceuticals Inc., Usa on February 25, 2015 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 68462-295-90?

    The 11-digit format is 68462029590. 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
    5-3-268462-295-905-4-268462-0295-90