NDC Package 24658-172-30 Diltiazem Hydrochloride

View Billable Units, 11-Digit Format, RxNorm

Package Information
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:

24658-172-30

Package Description:

30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE

Product Code:

24658-172

Proprietary Name:

Diltiazem Hydrochloride

Usage Information:

Diltiazem is contraindicated in (1) patients with sick sinus syndrome except in the presence of a functioning ventricular pacemaker, (2) patients with second- or third-degree AV block except in the presence of a functioning ventricular pacemaker, (3) patients with severe hypotension (less than 90 mm Hg systolic),(4) patients who have demonstrated hypersensitivity to the drug, and (5) patients with acute myocardial infarction and pulmonary congestion documented by x-ray on admission.

11-Digit NDC Billing Format:

24658017230

Billing Unit:

EA - Billing unit of "each" is used when the product is dispensed in discreet units.

NDC to RxNorm Crosswalk:

30 EA

NDC to RxNorm Crosswalk:

RxCUI: 830795 - dilTIAZem hydrochloride 360 MG 24HR Extended Release Oral Capsule

RxCUI: 830795 - 24 HR diltiazem hydrochloride 360 MG Extended Release Oral Capsule

RxCUI: 830795 - diltiazem hydrochloride 360 MG 24 HR Extended Release Oral Capsule

RxCUI: 830801 - dilTIAZem hydrochloride 300 MG 24HR Extended Release Oral Capsule

RxCUI: 830801 - 24 HR diltiazem hydrochloride 300 MG Extended Release Oral Capsule

Labeler Name:

Puracap Laboratories Llc

Sample Package:

Start Marketing Date:

11-01-2016

Listing Expiration Date:

12-31-2020

Exclude Flag:

Code Structure:

24658 - Puracap Laboratories Llc
- 24658-172 - Diltiazem Hydrochloride
  - 24658-172-30 - 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE

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 24658-172-30?

The NDC Packaged Code 24658-172-30 is assigned to a package of 30 capsule, extended release in 1 bottle of Diltiazem Hydrochloride, labeled by Puracap Laboratories Llc. The product's dosage form is and is administered via form.

Is NDC 24658-172 included in the NDC Directory?

No, Diltiazem Hydrochloride with product code 24658-172 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Puracap Laboratories Llc on November 01, 2016 and its listing in the NDC Directory is set to expire on December 31, 2020 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 24658-172-30?

The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 30.

What is the 11-digit format for NDC 24658-172-30?

The 11-digit format is 24658017230. 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 Format	10-Digit Original Code	11-Digit Format	11-Digit Code
5-3-2	24658-172-30	5-4-2	24658-0172-30

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