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  5. NDC Package Code: 45737-261-16 Biocotron Ped

NDC Package 45737-261-16 Biocotron Ped

Dextromethorphan Hbr,Guaifenesin,Phenylephrine Hcl Liquid Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

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:
45737-261-16
Package Description:
473 mL in 1 BOTTLE
Product Code:
45737-261
Proprietary Name:
Biocotron Ped
Non-Proprietary Name:
Dextromethorphan Hbr, Guaifenesin, Phenylephrine Hcl
Substance Name:
Dextromethorphan Hydrobromide; Guaifenesin; Phenylephrine Hydrochloride
Usage Information:
Usesnon-narcotic cough suppressant which temporarily calms cough due to minor throat and bronchial irritation as may occur with the common coldcalms the cough control center and relieves coughinghelps loosen phlegm (mucus) and thin bronchial secretions to drain bronchial tubes and make coughs more productive.temporarily relieves nasal congestion due to the common coldhelps decongest sinus openings and passages; temporarily relieves sinus congestion and pressure
11-Digit NDC Billing Format:
45737026116
NDC to RxNorm Crosswalk:
  • RxCUI: 1372451 - dextromethorphan HBr 15 MG / guaiFENesin 350 MG / phenylephrine HCl 10 MG in 5 mL Oral Solution
  • RxCUI: 1372451 - dextromethorphan hydrobromide 3 MG/ML / guaifenesin 70 MG/ML / phenylephrine hydrochloride 2 MG/ML Oral Solution
  • RxCUI: 1372451 - dextromethorphan HBr 15 MG / guaifenesin 350 MG / phenylephrine HCl 10 MG per 5 ML Oral Solution
Product Type:
Human Otc Drug
Labeler Name:
Advanced Generic Corporation
Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
M012
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
03-01-2015
Listing Expiration Date:
12-31-2025
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 45737-261-16?

The NDC Packaged Code 45737-261-16 is assigned to a package of 473 ml in 1 bottle of Biocotron Ped, a human over the counter drug labeled by Advanced Generic Corporation. The product's dosage form is liquid and is administered via oral form.

Is NDC 45737-261 included in the NDC Directory?

Yes, Biocotron Ped with product code 45737-261 is active and included in the NDC Directory. The product was first marketed by Advanced Generic Corporation on March 01, 2015 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 45737-261-16?

The 11-digit format is 45737026116. 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
5-3-245737-261-165-4-245737-0261-16