0121-4809 NDC - GUAIFENESIN DM ()

Drug Information

Product NDC: 0121-4809

Proprietary Name: Guaifenesin DM

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Name:	Pharmaceutical Associates, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:	5/17/2010

No.	Package Code	Package Description	Billing Unit
1	0121-4809-05	4 TRAY in 1 CASE (0121-4809-05) / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE
2	0121-4809-10	4 TRAY in 1 CASE (0121-4809-10) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE

Field Name	Field Value	Definition
PRODUCT NDC	0121-4809	The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAME	Guaifenesin DM	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	5/17/2010	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Pharmaceutical Associates, Inc.	Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/1/2023