Egaten Tablet
NDC Package 0078-0937-91
Package Information
Egaten (triclabendazole) tablets is eGATEN™ is indicated for the treatment of fascioliasis in patients 6 years of age and older. This formulation utilizes a tablet delivery system. Marketed by Novartis Pharmaceuticals Corporation, this product is identified by NDC 0078-0937 and is authorized under FDA application NDA208711.
Identification & Billing
- RxCUI: 2118606 - triclabendazole 250 MG Oral Tablet
- RxCUI: 2118612 - Egaten 250 MG Oral Tablet
- RxCUI: 2118612 - triclabendazole 250 MG Oral Tablet [Egaten]
Clinical Specifications
- Anthelmintic - [EPC] (Established Pharmacologic Class)
- Anthelmintics - [CS]
- Cytochrome P450 1A2 Inhibitors - [MoA] (Mechanism of Action)
- Cytochrome P450 2A6 Inhibitors - [MoA] (Mechanism of Action)
- Cytochrome P450 2B6 Inhibitors - [MoA] (Mechanism of Action)
- Cytochrome P450 2C19 Inhibitors - [MoA] (Mechanism of Action)
- Cytochrome P450 2C8 Inhibitors - [MoA] (Mechanism of Action)
- Cytochrome P450 2C9 Inhibitors - [MoA] (Mechanism of Action)
- Cytochrome P450 2D6 Inhibitors - [MoA] (Mechanism of Action)
- Cytochrome P450 3A Inhibitors - [MoA] (Mechanism of Action)
Regulatory & Marketing
Hierarchy Structure
- 0078 - Novartis Pharmaceuticals Corporation
- 0078-0937 - Egaten
- 0078-0937-91 - 4 TABLET in 1 BLISTER PACK
- 0078-0937 - Egaten
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 0078-0937-91 identifies a specific commercial package of 4 tablet in 1 blister pack of Egaten, 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 tablet is formulated for oral use and contains triclabendazole 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 February 13, 2019. The current certification is valid through December 31, 2027.
How is this Novartis Pharmaceuticals Corporation product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 00078093791. 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.