NDC Package 54859-606-01 Tusnel-dm Pediatric

Dextromethorphan Hbr,Guaifenesin,Phenylephrine Hcl Solution/ Drops Oral - View Billable Units, 11-Digit Format, RxNorm

Package Information

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:
54859-606-01
Package Description:
30 mL in 1 BOTTLE, DROPPER
Product Code:
Proprietary Name:
Tusnel-dm Pediatric
Non-Proprietary Name:
Dextromethorphan Hbr, Guaifenesin, Phenylephrine Hcl
Substance Name:
Dextromethorphan Hydrobromide; Guaifenesin; Phenylephrine Hydrochloride
Usage Information:
UsesTemporary relief of cough due to minor throat and bronchial irritationTemporarily relieves nasal congestion due to the common cold and thin bronchial secretions to make coughs more productiveHelps loosen phlegm (mucus) and thin bronchial secretions to make cough more productive.
11-Digit NDC Billing Format:
54859060601
NDC to RxNorm Crosswalk:
  • RxCUI: 2268062 - dextromethorphan HBr 2.5 MG / guaiFENesin 25 MG / phenylephrine HCl 1.25 MG in 1 mL Oral Solution
  • RxCUI: 2268062 - dextromethorphan hydrobromide 2.5 MG/ML / guaifenesin 25 MG/ML / phenylephrine hydrochloride 1.25 MG/ML Oral Solution
  • RxCUI: 2268062 - dextromethorphan hydrobromide 2.5 MG / guaifenesin 25 MG / phenylephrine hydrochloride 1.25 MG per 1 mL Oral Solution
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Llorens Pharmaceuticals International Division
    Dosage Form:
    Solution/ Drops - A solution which is usually administered in a drop-wise fashion.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    FDA Application Number:
    part341
    Marketing Category:
    OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
    Start Marketing Date:
    08-01-2019
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Code Structure:

    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 54859-606-01?

    The NDC Packaged Code 54859-606-01 is assigned to a package of 30 ml in 1 bottle, dropper of Tusnel-dm Pediatric, a human over the counter drug labeled by Llorens Pharmaceuticals International Division. The product's dosage form is solution/ drops and is administered via oral form.

    Is NDC 54859-606 included in the NDC Directory?

    Yes, Tusnel-dm Pediatric with product code 54859-606 is active and included in the NDC Directory. The product was first marketed by Llorens Pharmaceuticals International Division on August 01, 2019 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 54859-606-01?

    The 11-digit format is 54859060601. 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 Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-254859-606-015-4-254859-0606-01