NDC Package 49963-813-01 Brontuss SF

View Billable Units, 11-Digit Format, RxNorm

Package Information
Other Packages
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:

49963-813-01

Package Description:

30 mL in 1 BOTTLE

Product Code:

49963-813

Proprietary Name:

Brontuss SF

Usage Information:

Do not exceed recommended dosage.Adults and Children 12 years ofage and over:1 teaspoonful (5 mL) every 4 hours, not toexceed 6 doses in a 24 hour period.Children 6 to under 12 years of age:1/2 teaspoonful (2.5 mL) every 4 hours, not to exceed 6 doses in a 24 hour period.Children under 6 years of age:Consult a doctor

11-Digit NDC Billing Format:

49963081301

NDC to RxNorm Crosswalk:

RxCUI: 1251031 - dextromethorphan HBr 15 MG / guaiFENesin 300 MG / phenylephrine HCl 10 MG in 5 mL Oral Solution

RxCUI: 1251031 - dextromethorphan hydrobromide 3 MG/ML / guaifenesin 60 MG/ML / phenylephrine hydrochloride 2 MG/ML Oral Solution

RxCUI: 1251031 - dextromethorphan HBr 15 MG / guaifenesin 300 MG / phenylephrine HCl 10 MG per 5 ML Oral Solution

Labeler Name:

Portal Inc.

Sample Package:

Start Marketing Date:

03-16-2010

Listing Expiration Date:

12-31-2017

Exclude Flag:

Code Structure:

49963 - Portal Inc.
- 49963-813 - Brontuss
  - 49963-813-01 - 30 mL in 1 BOTTLE

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.

Other Product Packages

The following packages are also available for this product:

NDC Package Code	Package Description
49963-813-04	118 mL in 1 BOTTLE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 49963-813-01?

The NDC Packaged Code 49963-813-01 is assigned to a package of 30 ml in 1 bottle of Brontuss SF, labeled by Portal Inc.. The product's dosage form is and is administered via form.

Is NDC 49963-813 included in the NDC Directory?

No, Brontuss SF with product code 49963-813 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Portal Inc. on March 16, 2010 and its listing in the NDC Directory is set to expire on December 31, 2017 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 49963-813-01?

The 11-digit format is 49963081301. 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	49963-813-01	5-4-2	49963-0813-01

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