Montelukast
NDC Package 68071-2425-9
Package Information
Montelukast is • Hypersensitivity to any component of this product. Marketed by Nucare Pharmaceuticals,inc., this product is identified by NDC 68071-2425 and is authorized under FDA application ANDA202843.
Identification & Billing
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 68071 - Nucare Pharmaceuticals,inc.
- 68071-2425 - Montelukast
- 68071-2425-9 - 90 TABLET, FILM COATED in 1 BOTTLE
- 68071-2425 - Montelukast
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 68071-2425-9 identifies a specific commercial package of 90 tablet, film coated in 1 bottle of Montelukast, labeled by Nucare Pharmaceuticals,inc.. This is formulated for use and contains as the active substance.
Is this product currently listed with the FDA?
This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Nucare Pharmaceuticals,inc. on September 10, 2014. The current certification is valid through July 31, 2024.
How is this Nucare Pharmaceuticals,inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 68071242509. 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.