Guaifenesin, Dextromethorphan Hbr Capsule, Liquid Filled
NDC Package 69729-783-02

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Guaifenesin, Dextromethorphan Hbr capsules is helps loosen phlegm (mucus) Helps thin bronchial secretions to make coughs more productive. This formulation utilizes a capsule, liquid filled delivery system. Marketed by Opmx Llc, this product is identified by NDC 69729-783 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
69729-783-02
Package Description
2 BLISTER PACK in 1 CARTON / 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product Code
69729-783
11-Digit Billing Format
69729078302
RxNorm Crosswalk
  • RxCUI: 1661740 - dextromethorphan HBr 20 MG / guaiFENesin 400 MG Oral Capsule
  • RxCUI: 1661740 - dextromethorphan hydrobromide 20 MG / guaifenesin 400 MG Oral Capsule

Clinical Specifications

Proprietary Name
Guaifenesin, Dextromethorphan Hbr
Non-Proprietary Name
Guaifenesin, Dextromethorphan Hbr
Substance Name
Dextromethorphan Hydrobromide; Guaifenesin
Dosage Form
Capsule, Liquid Filled - A solid dosage form in which the drug is enclosed within a soluble, gelatin shell which is plasticized by the addition of a polyol, such as sorbitol or glycerin, and is therefore of a somewhat thicker consistency than that of a hard shell capsule; typically, the active ingredients are dissolved or suspended in a liquid vehicle.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
Helps loosen phlegm (mucus) Helps thin bronchial secretions to make coughs more productive

Regulatory & Marketing

Labeler Name
Opmx Llc
Product Type
Human Otc Drug
FDA Application #
M012
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
02-18-2019
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 69729-783-02 identifies a specific commercial package of 2 blister pack in 1 carton / 10 capsule, liquid filled in 1 blister pack of Guaifenesin, Dextromethorphan Hbr, a human over the counter drug labeled by Opmx Llc. This capsule, liquid filled is formulated for oral use and contains dextromethorphan hydrobromide; guaifenesin as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Opmx Llc on February 18, 2019. The current certification is valid through December 31, 2026.

How is this Opmx Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 69729078302. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
69729-783-02
11-Digit CMS (5-4-2)
69729-0783-02

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.