NDC Package 21695-803-30 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:

21695-803-30

Package Description:

30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE

Product Code:

21695-803

Proprietary Name:

Diltiazem Hydrochloride

Usage Information:

Diltiazem hydrochloride extended-release capsules are indicated for the treatment of hypertension. They may be used alone or in combination with other antihypertensive medications.Diltiazem hydrochloride extended-release capsules are indicated for the management of chronic stable angina and angina due to coronary artery spasm.

11-Digit NDC Billing Format:

21695080330

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: 830837 - dilTIAZem HCl 240 MG 24HR Extended Release Oral Capsule

RxCUI: 830837 - 24 HR diltiazem hydrochloride 240 MG Extended Release Oral Capsule

RxCUI: 830837 - diltiazem HCl 240 MG 24 HR Extended Release Oral Capsule

RxCUI: 830845 - dilTIAZem HCl 180 MG 24HR Extended Release Oral Capsule

RxCUI: 830845 - 24 HR diltiazem hydrochloride 180 MG Extended Release Oral Capsule

Labeler Name:

Rebel Distributors Corp

Sample Package:

Start Marketing Date:

12-20-1999

Listing Expiration Date:

12-31-2017

Exclude Flag:

Code Structure:

21695 - Rebel Distributors Corp
- 21695-803 - Diltiazem Hydrochloride
  - 21695-803-30 - 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 21695-803-30?

The NDC Packaged Code 21695-803-30 is assigned to a package of 30 capsule, extended release in 1 bottle of Diltiazem Hydrochloride, labeled by Rebel Distributors Corp. The product's dosage form is and is administered via form.This product is billed for "EA" each discreet unit and contains an estimated amount of 30 billable units per package.

Is NDC 21695-803 included in the NDC Directory?

No, Diltiazem Hydrochloride with product code 21695-803 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Rebel Distributors Corp on December 20, 1999 and its listing in the NDC Directory is set to expire on December 31, 2017 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 21695-803-30?

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 21695-803-30?

The 11-digit format is 21695080330. 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	21695-803-30	5-4-2	21695-0803-30

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