NDC 0121-4809-10 Guaifenesin Dm

NDC Package Code 0121-4809-10

The NDC Code 0121-4809-10 is assigned to a package of 4 tray in 1 case > 10 cup, unit-dose in 1 tray > 10 ml in 1 cup, unit-dose of Guaifenesin Dm, labeled by Pharmaceutical Associates, Inc.. The product's dosage form is and is administered via form.

Field Name Field Value
NDC Code 0121-4809-10
Package Description 4 TRAY in 1 CASE > 10 CUP, UNIT-DOSE in 1 TRAY > 10 mL in 1 CUP, UNIT-DOSE
Proprietary Name Guaifenesin Dm What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
11-Digit NDC Billing Format 00121480910 NDC Format for Billing
For insurance billing purposes the Centers for Medicare & Medicaid Services (CMS) created an 11 digit NDC derivative identifier. If the NDC Package code is less than 11 digits the code must be padded with leading zeros. The leading zeros must be added to the appropriate segment to create a 5-4-2 configuration.
RxNorm Crosswalk1046631 - RxCUI What is RxNorm?
The RxNorm crosswalk provides a normalized naming system for generic and branded drugs by assigning unique concept identifiers (RxCUI) to each NDC.
Labeler Name Pharmaceutical Associates, Inc.
Sample Package No Sample Package?
This field Indicates whether this package is a sample packaging or not.
Start Marketing Date 05-17-2010 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
Listing Expiration Date 12-31-2017 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.
Exclude Flag I What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".
This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Code Structure

  • 0121 - Pharmaceutical Associates, Inc.
    • 0121-4809 - Guaifenesin Dm
      • 0121-4809-10 - 4 TRAY in 1 CASE

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 Guaifenesin Dm with product NDC 0121-4809.

NDC Package CodePackage Description
0121-4809-054 TRAY in 1 CASE > 10 CUP, UNIT-DOSE in 1 TRAY > 5 mL in 1 CUP, UNIT-DOSE

* Please review the disclaimer below.