Tasigna Capsule
NDC Package 0078-0592-87
Package Information
Tasigna (nilotinib) capsules is nilotinib is used to treat a certain type of blood cancer (chronic myelogenous leukemia-CML). This formulation utilizes a capsule delivery system. Marketed by Novartis Pharmaceuticals Corporation, this product is identified by NDC 0078-0592 and is authorized under FDA application NDA022068.
Identification & Billing
- RxCUI: 1002300 - Tasigna 150 MG Oral Capsule
- RxCUI: 1002300 - nilotinib 150 MG Oral Capsule [Tasigna]
- RxCUI: 1002300 - Tasigna (as nilotinib HCl) 150 MG Oral Capsule
- RxCUI: 2002717 - nilotinib 50 MG Oral Capsule
- RxCUI: 2002717 - nilotinib (as nilotinib hydrochloride) 50 MG Oral Capsule
Clinical Specifications
- Bcr-Abl Tyrosine Kinase Inhibitors - [MoA] (Mechanism of Action)
- Cytochrome P450 2B6 Inducers - [MoA] (Mechanism of Action)
- Cytochrome P450 2C8 Inducers - [MoA] (Mechanism of Action)
- Cytochrome P450 2C8 Inhibitors - [MoA] (Mechanism of Action)
- Cytochrome P450 2D6 Inhibitors - [MoA] (Mechanism of Action)
- Kinase Inhibitor - [EPC] (Established Pharmacologic Class)
- P-Glycoprotein Inhibitors - [MoA] (Mechanism of Action)
- UGT1A1 Inhibitors - [MoA] (Mechanism of Action)
Regulatory & Marketing
Hierarchy Structure
- 0078 - Novartis Pharmaceuticals Corporation
- 0078-0592 - Tasigna
- 0078-0592-87 - 4 BLISTER PACK in 1 CARTON / 28 CAPSULE in 1 BLISTER PACK
- 0078-0592 - Tasigna
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 (0078-0592). 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 0078-0592-87 identifies a specific commercial package of 4 blister pack in 1 carton / 28 capsule in 1 blister pack of Tasigna, a human prescription drug labeled by Novartis Pharmaceuticals Corporation. This product is billed for "EA" each discreet unit and contains an estimated amount of 4 billable units per package. This capsule is formulated for oral use and contains nilotinib hydrochloride monohydrate 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 Novartis Pharmaceuticals Corporation on October 29, 2007. The current certification is valid through December 31, 2026.
What are the primary indications for this medication?
Nilotinib is used to treat a certain type of blood cancer (chronic myelogenous leukemia-CML). It works by slowing or stopping the growth of cancer cells.
How is this Novartis Pharmaceuticals Corporation product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 00078059287. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 4 total billable units per package. 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 Labeler segment to maintain the 5-4-2 structure.