Tussionex Pennkinetic
NDC Package 53014-548-01

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.

Tussionex Pennkinetic is extended-Release Suspension is indicated for relief of cough and upper respiratory symptoms associated with allergy or a cold in adults and children 6 years of age and older. Marketed by Unither Manufacturing Llc, this product is identified by NDC 53014-548 and is authorized under FDA application NDA019111.

Identification & Billing

NDC Package Code
53014-548-01
Package Description
1 BOTTLE, PLASTIC in 1 CARTON / 115 mL in 1 BOTTLE, PLASTIC
Product Code
53014-548
11-Digit Billing Format
53014054801
Billing Unit
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
RxNorm Crosswalk
  • RxCUI: 1087459 - HYDROcodone polistirex 10 MG / chlorpheniramine polistirex 8 MG in 5 mL 12HR Extended Release Oral Suspension
  • RxCUI: 1087459 - 12 HR chlorpheniramine polistirex 1.6 MG/ML / hydrocodone polistirex 2 MG/ML Extended Release Suspension
  • RxCUI: 1087459 - hydrocodone polistirex 10 MG / chlorpheniramine polistirex 8 MG per 5 ML 12HR Extended Release Oral Suspension
  • RxCUI: 1087463 - Tussionex Pennkinetic 10 MG / 8 MG in 5 mL 12HR Extended Release Oral Suspension
  • RxCUI: 1087463 - 12 HR chlorpheniramine polistirex 1.6 MG/ML / hydrocodone polistirex 2 MG/ML Extended Release Suspension [Tussionex]

Clinical Specifications

Proprietary Name
Tussionex Pennkinetic
Dosage Form
-
Usage Information
TUSSIONEX Pennkinetic Extended-Release Suspension is indicated for relief of cough and upper respiratory symptoms associated with allergy or a cold in adults and children 6 years of age and older.

Regulatory & Marketing

Labeler Name
Unither Manufacturing Llc
FDA Application #
NDA019111
Marketing Category
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date
12-31-1987
Listing Expiration
12-31-2018
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 53014-548-01 identifies a specific commercial package of 1 bottle, plastic in 1 carton / 115 ml in 1 bottle, plastic of Tussionex Pennkinetic, labeled by Unither Manufacturing Llc. 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 Unither Manufacturing Llc on December 31, 1987. The current certification is valid through December 31, 2018.

How is this Unither Manufacturing Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 53014054801. Quantities are measured in per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.. 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)
53014-548-01
11-Digit CMS (5-4-2)
53014-0548-01

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