Guaifenesin
NDC Package 49349-511-02

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

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Guaifenesin is do not exceed 6 doses in 24 hourstake with a full glass of wateradults and children 12 years of age and over 1 to 2 tablets every 4 hours children 6 to under 12 years of age ½ to 1 tablet every 4 hours children under 6 years of ageconsult a physician. Marketed by Remedyrepack Inc., this product is identified by NDC 49349-511 and is authorized under FDA application part341.

Identification & Billing

NDC Package Code
49349-511-02
Package Description
30 TABLET in 1 BLISTER PACK
Product Code
49349-511
11-Digit Billing Format
49349051102
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Guaifenesin
Dosage Form
-
Usage Information
Do not exceed 6 doses in 24 hourstake with a full glass of wateradults and children 12 years of age and over 1 to 2 tablets every 4 hours children 6 to under 12 years of age ½ to 1 tablet every 4 hours children under 6 years of ageconsult a physician

Regulatory & Marketing

Labeler Name
Remedyrepack Inc.
FDA Application #
part341
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
08-12-2010
Listing Expiration
12-31-2018
Exclude Flag
I
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 49349-511-02 identifies a specific commercial package of 30 tablet in 1 blister pack of Guaifenesin, labeled by Remedyrepack Inc.. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Remedyrepack Inc. on August 12, 2010. The current certification is valid through December 31, 2018.

How is this Remedyrepack Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 49349051102. 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)
49349-511-02
11-Digit CMS (5-4-2)
49349-0511-02

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