NDC Package 85722-0001-4 Dextromethorphan Hydrobromide And Guaifenesin

Syrup Oral - View Billable Units, 11-Digit Format, RxNorm

Package Information
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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:

85722-0001-4

Package Description:

118 mL in 1 BOTTLE

Product Code:

85722-0001

Proprietary Name:

Dextromethorphan Hydrobromide And Guaifenesin

Non-Proprietary Name:

Dextromethorphan Hydrobromide And Guaifenesin

Substance Name:

Dextromethorphan Hydrobromide; Guaifenesin

Usage Information:

Take evey 4 hoursdo not take more than 6 doses in any 24-hour periodmeasure only with dosing cup providedkeep dosing cup with productAgeDoseAdults and children 12 years and over2 teaspoonful (10 mL)Children 6 to under 12 years1 teaspoonful (5 mL)Children under 6 yearsAsk a doctor

11-Digit NDC Billing Format:

85722000104

Product Type:

Human Otc Drug

Labeler Name:

Kjd Pharma Private Limited

Dosage Form:

Syrup - An oral solution containing high concentrations of sucrose or other sugars; the term has also been used to include any other liquid dosage form prepared in a sweet and viscid vehicle, including oral suspensions.

Administration Route(s):

Oral - Administration to or by way of the mouth.

Active Ingredient(s):

Pharmacologic Class(es):

Sample Package:

FDA Application Number:

M012

Marketing Category:

OTC MONOGRAPH DRUG -

Start Marketing Date:

02-01-2021

Listing Expiration Date:

12-31-2026

Exclude Flag:

Code Structure:

85722 - Kjd Pharma Private Limited
- 85722-0001 - Dextromethorphan Hydrobromide And Guaifenesin
  - 85722-0001-4 - 118 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
85722-0001-6	473 mL in 1 BOTTLE
85722-0001-8	236 mL in 1 BOTTLE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 85722-0001-4?

The NDC Packaged Code 85722-0001-4 is assigned to a package of 118 ml in 1 bottle of Dextromethorphan Hydrobromide And Guaifenesin, a human over the counter drug labeled by Kjd Pharma Private Limited. The product's dosage form is syrup and is administered via oral form.

Is NDC 85722-0001 included in the NDC Directory?

Yes, Dextromethorphan Hydrobromide And Guaifenesin with product code 85722-0001 is active and included in the NDC Directory. The product was first marketed by Kjd Pharma Private Limited on February 01, 2021 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 85722-0001-4?

The 11-digit format is 85722000104. 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 5-4-1 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
5-4-1	85722-0001-4	5-4-2	85722-0001-04

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