NDC Package 50228-484-05 Diltiazem Hydrochloride

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:
50228-484-05
Package Description:
500 TABLET in 1 BOTTLE
Product Code:
Proprietary Name:
Diltiazem Hydrochloride
Non-Proprietary Name:
Diltiazem Hydrochloride
Substance Name:
Diltiazem Hydrochloride
Usage Information:
Diltiazem hydrochloride tablets are indicated for the management of chronic stable angina and angina due to coronary artery spasm.
11-Digit NDC Billing Format:
50228048405
NDC to RxNorm Crosswalk:
  • RxCUI: 831054 - dilTIAZem hydrochloride 120 MG Oral Tablet
  • RxCUI: 831054 - diltiazem hydrochloride 120 MG Oral Tablet
  • RxCUI: 831102 - dilTIAZem HCl 90 MG Oral Tablet
  • RxCUI: 831102 - diltiazem hydrochloride 90 MG Oral Tablet
  • RxCUI: 831103 - dilTIAZem hydrochloride 60 MG Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Sciegen 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:
    ANDA216521
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    09-26-2022
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    50228-484-01100 TABLET in 1 BOTTLE
    50228-484-3030 TABLET in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 50228-484-05?

    The NDC Packaged Code 50228-484-05 is assigned to a package of 500 tablet in 1 bottle of Diltiazem Hydrochloride, a human prescription drug labeled by Sciegen Pharmaceuticals, Inc. The product's dosage form is tablet and is administered via oral form.

    Is NDC 50228-484 included in the NDC Directory?

    Yes, Diltiazem Hydrochloride with product code 50228-484 is active and included in the NDC Directory. The product was first marketed by Sciegen Pharmaceuticals, Inc on September 26, 2022 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 50228-484-05?

    The 11-digit format is 50228048405. 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
    5-3-250228-484-055-4-250228-0484-05