Tusslin
NDC Package 52083-623-01

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

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Tusslin is other information Tamper Evident Feature: Do not use if cap seal is torn, broken or missing.Store at controlled room temperature 15-30°C (59-86°F).Avoid excessive heat and humidity. Marketed by Kramer Novis, this product is identified by NDC 52083-623 and is authorized under FDA application part341.

Identification & Billing

NDC Package Code
52083-623-01
Package Description
30 mL in 1 BOTTLE, DROPPER
Product Code
52083-623
11-Digit Billing Format
52083062301
RxNorm Crosswalk
  • RxCUI: 1487369 - dextromethorphan HBr 7.5 MG / guaiFENesin 88 MG / phenylephrine HCl 2.5 MG in 1 mL Oral Solution
  • RxCUI: 1487369 - dextromethorphan hydrobromide 7.5 MG/ML / guaifenesin 88 MG/ML / phenylephrine hydrochloride 2.5 MG/ML Oral Solution
  • RxCUI: 1487369 - dextromethorphan HBr 7.5 MG / guaifenesin 88 MG / phenylephrine HCl 2.5 MG per 1 ML Oral Solution

Clinical Specifications

Proprietary Name
Tusslin Pediatric
Dosage Form
-
Usage Information
Other information Tamper Evident Feature: Do not use if cap seal is torn, broken or missing.Store at controlled room temperature 15-30°C (59-86°F).Avoid excessive heat and humidity.

Regulatory & Marketing

Labeler Name
Kramer Novis
FDA Application #
part341
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
01-27-2014
Listing Expiration
12-31-2024
Exclude Flag
I
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 52083-623-01 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Tusslin Pediatric, labeled by Kramer Novis. 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 Kramer Novis on January 27, 2014. The current certification is valid through December 31, 2024.

How is this Kramer Novis product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 52083062301. 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)
52083-623-01
11-Digit CMS (5-4-2)
52083-0623-01

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