NDC Package 83720-501-08 Guaifenesin And Dextromethorphan Hydrobromide

Guaifenesin And Dextromethorphan Hydrobromide Syrup Liquid 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:
83720-501-08
Package Description:
237 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Guaifenesin And Dextromethorphan Hydrobromide
Non-Proprietary Name:
Guaifenesin And Dextromethorphan Hydrobromide Syrup
Substance Name:
Dextromethorphan Hydrobromide; Guaifenesin
Usage Information:
Do not exceed recommended dosage.adults and children 12 years and over:2 teaspoonfuls (10 mL) every 4 hours, not to exceed 12 teaspoonfuls in 24 hours or as directed by a doctorchildren 6 to under 12 years of age:1 teaspoonful (5 mL) every 4 hours, not to exceed 6 teaspoonfuls in 24 hours or as directed by a doctorchildren under 6 years of age:consult a physician
11-Digit NDC Billing Format:
83720050108
NDC to RxNorm Crosswalk:
  • RxCUI: 996520 - dextromethorphan HBr 20 MG / guaiFENesin 200 MG in 10 mL Oral Solution
  • RxCUI: 996520 - dextromethorphan hydrobromide 2 MG/ML / guaifenesin 20 MG/ML Oral Solution
  • RxCUI: 996520 - dextromethorphan hydrobromide 10 MG / guaifenesin 100 MG per 5 ML Oral Solution
  • RxCUI: 996520 - dextromethorphan hydrobromide 15 MG / guaifenesin 150 MG per 7.5 ML Oral Solution
  • RxCUI: 996520 - dextromethorphan hydrobromide 20 MG / guaifenesin 200 MG per 10 ML Oral Solution
Product Type:
Human Otc Drug
Labeler Name:
Oncor Pharmaceuticals
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.
Sample Package:
No
FDA Application Number:
M012
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
02-01-2025
Listing Expiration Date:
12-31-2026
Exclude Flag:
N

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.

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Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
83720-501-16473 mL in 1 BOTTLE

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Frequently Asked Questions

What is NDC 83720-501-08?

The NDC Packaged Code 83720-501-08 is assigned to a package of 237 ml in 1 bottle of Guaifenesin And Dextromethorphan Hydrobromide, a human over the counter drug labeled by Oncor Pharmaceuticals. The product's dosage form is liquid and is administered via oral form.

Is NDC 83720-501 included in the NDC Directory?

Yes, Guaifenesin And Dextromethorphan Hydrobromide with product code 83720-501 is active and included in the NDC Directory. The product was first marketed by Oncor Pharmaceuticals on February 01, 2025 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 83720-501-08?

The 11-digit format is 83720050108. 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
5-3-283720-501-085-4-283720-0501-08