Tussi Pres Pediatric Syrup
NDC Package 52083-232-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

Tussi Pres Pediatric (guaifenesin, phenylephrine hcl, dextromethorphan hydrobromide) syrups is helps loosen phlegm (mucus) and thin bronchial secretions to drainbronchial tubestemporarily relieves these symptoms occurring with cold:nasal congestioncough due to minor throat and bronchial irritation. This formulation utilizes a syrup delivery system. Marketed by Kramer Novis, this product is identified by NDC 52083-232 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
52083-232-01
Package Description
30 mL in 1 BOTTLE
Product Code
52083-232
11-Digit Billing Format
52083023201
RxNorm Crosswalk
  • RxCUI: 1119541 - dextromethorphan HBr 5 MG / guaiFENesin 75 MG / phenylephrine HCl 2.5 MG in 5 mL Oral Solution
  • RxCUI: 1119541 - dextromethorphan hydrobromide 1 MG/ML / guaifenesin 15 MG/ML / phenylephrine hydrochloride 0.5 MG/ML Oral Solution
  • RxCUI: 1119541 - dextromethorphan hydrobromide 5 MG / guaifenesin 75 MG / phenylephrine hydrochloride 2.5 MG per 5 ML Oral Solution

Clinical Specifications

Proprietary Name
Tussi Pres Pediatric
Non-Proprietary Name
Guaifenesin, Phenylephrine Hcl, Dextromethorphan Hydrobromide
Substance Name
Dextromethorphan Hydrobromide; Guaifenesin; Phenylephrine Hydrochloride
Dosage Form
Syrup - An oral solution containing high concentrations of sucrose or other sugars; the term has also been used to include any other liquid dosage form prepared in a sweet and viscid vehicle, including oral suspensions.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
Helps loosen phlegm (mucus) and thin bronchial secretions to drainbronchial tubestemporarily relieves these symptoms occurring with cold:nasal congestioncough due to minor throat and bronchial irritation

Regulatory & Marketing

Labeler Name
Kramer Novis
Product Type
Human Otc Drug
FDA Application #
M012
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
03-24-2011
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 (52083-232). Click a package code to view its specific billing and regulatory data.

52083-232-04
120 mL in 1 BOTTLE
52083-232-05
5 mL in 1 BOTTLE
52083-232-16
480 mL in 1 BOTTLE

* 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 52083-232-01 identifies a specific commercial package of 30 ml in 1 bottle of Tussi Pres Pediatric, a human over the counter drug labeled by Kramer Novis. This syrup is formulated for oral use and contains dextromethorphan hydrobromide; guaifenesin; phenylephrine 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 Kramer Novis on March 24, 2011. The current certification is valid through December 31, 2026.

How is this Kramer Novis product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 52083023201. 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:

10-Digit Format (5-3-2)
52083-232-01
11-Digit CMS (5-4-2)
52083-0232-01

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.