Conex Tablet
NDC Package 54859-702-60
Package Information
Conex (dexbrompheniramine maleate, pseudoephedrine hcl) tablets is other Information: Store at controlled room temperature 20 - 25 degree celsius (68 - 77 degree fahrenheit); excursions permitted to 15 - 30 degree celsius ( 59 - 86 degree fahrenheit) [ See USP Controlled Room Temperature] Tamper evident by imprinted heat seal under cap. This formulation utilizes a tablet delivery system. Marketed by Llorens Pharmaceuticals International Division, this product is identified by NDC 54859-702 and is authorized under FDA application M012.
Identification & Billing
- RxCUI: 1363513 - dexbrompheniramine maleate 2 MG / pseudoephedrine HCl 60 MG Oral Tablet
- RxCUI: 1363513 - dexbrompheniramine maleate 2 MG / pseudoephedrine hydrochloride 60 MG Oral Tablet
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 54859 - Llorens Pharmaceuticals International Division
- 54859-702 - Conex
- 54859-702-60 - 60 TABLET in 1 BOTTLE
- 54859-702 - Conex
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.
Frequently Asked Questions
What is the distribution configuration for this product package?
The code 54859-702-60 identifies a specific commercial package of 60 tablet in 1 bottle of Conex, a human over the counter drug labeled by Llorens Pharmaceuticals International Division. This product is billed for "EA" each discreet unit and contains an estimated amount of 60 billable units per package. This tablet is formulated for oral use and contains dexbrompheniramine maleate; pseudoephedrine 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 Llorens Pharmaceuticals International Division on November 01, 2007. The current certification is valid through December 31, 2026.
How is this Llorens Pharmaceuticals International Division product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 54859070260. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 60 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 Product segment to maintain the 5-4-2 structure.