Cartia Capsule, Extended Release
NDC Package 71335-0879-2
Package Information
Cartia (diltiazem hydrochloride) capsules is diltiazem is used to treat high blood pressure (hypertension) and prevent chest pain (angina). This formulation utilizes a capsule, extended release delivery system. Marketed by Bryant Ranch Prepack, this product is identified by NDC 71335-0879 and is authorized under FDA application ANDA074752.
Identification & Billing
- 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
- RxCUI: 831255 - Cartia XT 180 MG 24HR Extended Release Oral Capsule, Once-A-Day
- RxCUI: 831255 - 24 HR diltiazem hydrochloride 180 MG Extended Release Oral Capsule [Cartia]
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 71335 - Bryant Ranch Prepack
- 71335-0879 - Cartia
- 71335-0879-2 - 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE
- 71335-0879 - Cartia
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 full disclaimer at the bottom of this page.
Other Available Packages
The following commercial packages are registered under the same Product NDC (71335-0879). Click a package code to view its specific billing and regulatory data.
* Please review the full disclaimer at the bottom of this page.
Frequently Asked Questions
What is the distribution configuration for this product package?
The code 71335-0879-2 identifies a specific commercial package of 90 capsule, extended release in 1 bottle of Cartia XT, a human prescription drug labeled by Bryant Ranch Prepack. This capsule, extended release is formulated for oral use and contains diltiazem hydrochloride as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Bryant Ranch Prepack on July 09, 1998. The current certification is valid through December 31, 2026.
What are the primary indications for this medication?
Diltiazem is used to treat high blood pressure (hypertension) and prevent chest pain (angina). Lowering high blood pressure helps prevent strokes, heart attacks, and kidney problems. When used regularly, diltiazem can decrease the number and severity of episodes of chest pain from angina. It may help increase your ability to exercise. Diltiazem is called a calcium channel blocker. It works by relaxing blood vessels in the body and heart so blood can flow more easily. Diltiazem also lowers your heart rate. These effects help the heart work less hard and lower blood pressure.
How is this Bryant Ranch Prepack product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 71335087902. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Package segment to maintain the 5-4-2 structure.