NDC Package 72162-1902-3 Diltiazem Hydrochloride

Diltiazem Hydrochloride Extended-release Tablets Tablet, 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:
72162-1902-3
Package Description:
30 TABLET, EXTENDED RELEASE in 1 BOTTLE
Product Code:
Proprietary Name:
Diltiazem Hydrochloride
Non-Proprietary Name:
Diltiazem Hydrochloride Extended-release Tablets
Substance Name:
Diltiazem Hydrochloride
Usage Information:
Diltiazem Hydrochloride Extended-Release Tablets are contraindicated in:•Patients with sick sinus syndrome except in the presence of a functioning ventricular pacemaker. •Patients with second- or third-degree AV block except in the presence of a functioning ventricular pacemaker.•Patients with hypotension (less than 90 mm Hg systolic).•Patients who have demonstrated hypersensitivity to the drug.•Patients with acute myocardial infarction and pulmonary.
11-Digit NDC Billing Format:
72162190203
NDC to RxNorm Crosswalk:
  • RxCUI: 830877 - dilTIAZem hydrochloride 180 MG 24HR Extended Release Oral Tablet
  • RxCUI: 830877 - 24 HR diltiazem hydrochloride 180 MG Extended Release Oral Tablet
  • RxCUI: 830877 - diltiazem hydrochloride 180 MG 24 HR Extended Release Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Bryant Ranch Prepack
    Dosage Form:
    Tablet, Extended Release - A solid dosage form containing a drug which allows at least a reduction in dosing frequency as compared to that drug presented in conventional dosage form.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    NDA021392
    Marketing Category:
    NDA AUTHORIZED GENERIC - A product marketed as a "generic" drug under an approved New Drug Application (NDA), rather than an Abbreviated New Drug Application (ANDA),.
    Start Marketing Date:
    02-06-2014
    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.

    Frequently Asked Questions

    What is NDC 72162-1902-3?

    The NDC Packaged Code 72162-1902-3 is assigned to a package of 30 tablet, extended release in 1 bottle of Diltiazem Hydrochloride, a human prescription drug labeled by Bryant Ranch Prepack. The product's dosage form is tablet, extended release and is administered via oral form.

    Is NDC 72162-1902 included in the NDC Directory?

    Yes, Diltiazem Hydrochloride with product code 72162-1902 is active and included in the NDC Directory. The product was first marketed by Bryant Ranch Prepack on February 06, 2014 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 72162-1902-3?

    The 11-digit format is 72162190203. 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 5-4-1 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
    5-4-172162-1902-35-4-272162-1902-03