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  5. NDC Package Code: 0187-0771-47 Cardizem

NDC Package 0187-0771-47 Cardizem

Diltiazem Hydrochloride Tablet, Coated Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

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:
0187-0771-47
Package Description:
100 TABLET, COATED in 1 BOTTLE
Product Code:
0187-0771
Proprietary Name:
Cardizem
Non-Proprietary Name:
Diltiazem Hydrochloride
Substance Name:
Diltiazem Hydrochloride
Usage Information:
Diltiazem is used to prevent chest pain (angina). It may help to increase your ability to exercise and decrease how often you may get angina attacks. Diltiazem is called a calcium channel blocker. It works by relaxing blood vessels in the body and heart and lowers the heart rate. Blood can flow more easily and your heart works less hard to pump blood.
11-Digit NDC Billing Format:
00187077147
NDC to RxNorm Crosswalk:
  • RxCUI: 831054 - dilTIAZem hydrochloride 120 MG Oral Tablet
  • RxCUI: 831054 - diltiazem hydrochloride 120 MG Oral Tablet
  • RxCUI: 831055 - Cardizem 120 MG Oral Tablet
  • RxCUI: 831055 - diltiazem hydrochloride 120 MG Oral Tablet [Cardizem]
  • RxCUI: 831102 - dilTIAZem HCl 90 MG Oral Tablet
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Bausch Health Us Llc
    Dosage Form:
    Tablet, Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is covered with a designated coating.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • DILTIAZEM HYDROCHLORIDE 30 mg/1
    • Pharmacologic Class(es):
  • Calcium Channel Antagonists - [MoA] (Mechanism of Action)
  • Calcium Channel Blocker - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    NDA018602
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    12-25-2010
    Listing Expiration Date:
    12-31-2024
    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 0187-0771-47?

    The NDC Packaged Code 0187-0771-47 is assigned to a package of 100 tablet, coated in 1 bottle of Cardizem, a human prescription drug labeled by Bausch Health Us Llc. The product's dosage form is tablet, coated and is administered via oral form.

    Is NDC 0187-0771 included in the NDC Directory?

    Yes, Cardizem with product code 0187-0771 is active and included in the NDC Directory. The product was first marketed by Bausch Health Us Llc on December 25, 2010 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 0187-0771-47?

    The 11-digit format is 00187077147. 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
    4-4-20187-0771-475-4-200187-0771-47