NDC Package 53014-548-01 Tussionex Pennkinetic

View Billable Units, 11-Digit Format, RxNorm

Package Information
Frequently Asked Questions

Package Information

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

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:

53014-548-01

Package Description:

1 BOTTLE, PLASTIC in 1 CARTON / 115 mL in 1 BOTTLE, PLASTIC

Product Code:

53014-548

Proprietary Name:

Tussionex Pennkinetic

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.

11-Digit NDC Billing Format:

53014054801

Billing Unit:

ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.

NDC to 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]

Labeler Name:

Unither Manufacturing Llc

Sample Package:

Start Marketing Date:

12-31-1987

Listing Expiration Date:

12-31-2018

Exclude Flag:

Code Structure:

53014 - Unither Manufacturing Llc
- 53014-548 - Tussionex Pennkinetic
  - 53014-548-01 - 1 BOTTLE, PLASTIC in 1 CARTON / 115 mL in 1 BOTTLE, PLASTIC

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 disclaimer below.

Frequently Asked Questions

What is NDC 53014-548-01?

The NDC Packaged Code 53014-548-01 is assigned to a package of 1 bottle, plastic in 1 carton / 115 ml in 1 bottle, plastic of Tussionex Pennkinetic, labeled by Unither Manufacturing Llc. The product's dosage form is and is administered via form.

Is NDC 53014-548 included in the NDC Directory?

No, Tussionex Pennkinetic with product code 53014-548 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Unither Manufacturing Llc on December 31, 1987 and its listing in the NDC Directory is set to expire on December 31, 2018 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 53014-548-01?

The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.

What is the 11-digit format for NDC 53014-548-01?

The 11-digit format is 53014054801. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format	10-Digit Original Code	11-Digit Format	11-Digit Code
5-3-2	53014-548-01	5-4-2	53014-0548-01

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