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  5. NDC Package Code: 53002-1521-0 Diltiazem Hydrochloride

NDC Package 53002-1521-0 Diltiazem Hydrochloride

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
53002-1521-0
Package Description:
100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE
Product Code:
53002-1521
Proprietary Name:
Diltiazem Hydrochloride
Usage Information:
DILT-XR [Diltiazem Hydrochloride Extended-Release Capsules, USP (Once-a-day dosage)] are indicated for the treatment of hypertension. Diltiazem hydrochloride may be used alone or in combination with other antihypertensive medications, such as diuretics.DILT-XR [Diltiazem Hydrochloride Extended-Release Capsules, USP (Once-a-day dosage)] are indicated for the management of chronic stable angina.
11-Digit NDC Billing Format:
53002152100
NDC to RxNorm Crosswalk:
  • RxCUI: 830845 - dilTIAZem HCl 180 MG 24HR Extended Release Oral Capsule
  • RxCUI: 830845 - 24 HR diltiazem hydrochloride 180 MG Extended Release Oral Capsule
  • RxCUI: 830845 - diltiazem HCl 180 MG 24 HR Extended Release Oral Capsule
Labeler Name:
Rpk Pharmaceuticals, Inc.
Sample Package:
No
FDA Application Number:
ANDA074943
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
07-30-2001
Listing Expiration Date:
12-31-2024
Exclude Flag:
I
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 53002-1521-0?

The NDC Packaged Code 53002-1521-0 is assigned to a package of 100 capsule, extended release in 1 bottle of Diltiazem Hydrochloride, labeled by Rpk Pharmaceuticals, Inc.. The product's dosage form is and is administered via form.

Is NDC 53002-1521 included in the NDC Directory?

No, Diltiazem Hydrochloride with product code 53002-1521 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Rpk Pharmaceuticals, Inc. on July 30, 2001 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 53002-1521-0?

The 11-digit format is 53002152100. 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
5-4-153002-1521-05-4-253002-1521-00