NDC Package 63739-016-10 Diltiazem Hydrochloride Extended-release

View Billable Units, 11-Digit Format, RxNorm

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

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:
63739-016-10
Package Description:
10 BLISTER PACK in 1 BOX, UNIT-DOSE / 10 CAPSULE, COATED, EXTENDED RELEASE in 1 BLISTER PACK
Product Code:
Proprietary Name:
Diltiazem Hydrochloride Extended-release
Usage Information:
Diltiazem hydrochloride extended-release capsules, USP is indicated for the treatment of hypertension. It may be used alone or in combination with other antihypertensive medications.Diltiazem hydrochloride extended-release capsules, USP is indicated for the management of chronic stable angina and angina due to coronary artery spasm.
11-Digit NDC Billing Format:
63739001610
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
10 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:
Mckesson Corporation Dba Sky Packaging
Sample Package:
No
FDA Application Number:
ANDA074984
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
10-01-2015
End Marketing Date:
11-30-2023
Listing Expiration Date:
11-30-2023
Exclude Flag:
D
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 63739-016-10?

The NDC Packaged Code 63739-016-10 is assigned to a package of 10 blister pack in 1 box, unit-dose / 10 capsule, coated, extended release in 1 blister pack of Diltiazem Hydrochloride Extended-release, labeled by Mckesson Corporation Dba Sky Packaging. The product's dosage form is and is administered via form.

Is NDC 63739-016 included in the NDC Directory?

No, Diltiazem Hydrochloride Extended-release with product code 63739-016 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Mckesson Corporation Dba Sky Packaging on October 01, 2015 and its listing in the NDC Directory is set to expire on November 30, 2023 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 63739-016-10?

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 10.

What is the 11-digit format for NDC 63739-016-10?

The 11-digit format is 63739001610. 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
5-3-263739-016-105-4-263739-0016-10