Cardene Iv Injection, Solution
NDC Package 43066-024-10
Package Information
Cardene Iv (nicardipine hydrochloride) injection is cardene® I.V. This formulation utilizes a injection, solution delivery system. Marketed by Baxter Healthcare Corporation, this product is identified by NDC 43066-024 and is authorized under FDA application NDA019734.
Identification & Billing
- RxCUI: 858599 - niCARdipine HCl 20 MG in 200 ML Injection
- RxCUI: 858599 - 200 ML nicardipine hydrochloride 0.1 MG/ML Injection
- RxCUI: 858599 - nicardipine hydrochloride 20 MG per 200 ML Injection
- RxCUI: 858601 - CARDENE 20 MG in 200 ML Injection
- RxCUI: 858601 - 200 ML nicardipine hydrochloride 0.1 MG/ML Injection [Cardene]
Clinical Specifications
- Calcium Channel Antagonists - [MoA] (Mechanism of Action)
- Cytochrome P450 2C19 Inhibitors - [MoA] (Mechanism of Action)
- Cytochrome P450 2C8 Inhibitors - [MoA] (Mechanism of Action)
- Cytochrome P450 2D6 Inhibitors - [MoA] (Mechanism of Action)
- Cytochrome P450 3A4 Inhibitors - [MoA] (Mechanism of Action)
- Dihydropyridine Calcium Channel Blocker - [EPC] (Established Pharmacologic Class)
- Dihydropyridines - [CS]
Regulatory & Marketing
Hierarchy Structure
- 43066 - Baxter Healthcare Corporation
- 43066-024 - Cardene Iv
- 43066-024-10 - 10 BAG in 1 CARTON / 200 mL in 1 BAG
- 43066-024 - Cardene Iv
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.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 43066-024-10 identifies a specific commercial package of 10 bag in 1 carton / 200 ml in 1 bag of Cardene Iv, a human prescription drug labeled by Baxter Healthcare Corporation. This injection, solution is formulated for intravenous use and contains nicardipine 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 Baxter Healthcare Corporation on January 30, 1992. The current certification is valid through December 31, 2027.
How is this Baxter Healthcare Corporation product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 43066002410. Quantities are measured in per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.. 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 Product segment to maintain the 5-4-2 structure.