Mucinex - 63824-023-28 - (Guaifenesin)

Alphabetical Index


Drug Information of Mucinex

Product NDC: 63824-023
Proprietary Name: Mucinex
Non Proprietary Name: Guaifenesin
Active Ingredient(s): 1200    mg/1 & nbsp;   Guaifenesin
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Mucinex

Product NDC: 63824-023
Labeler Name: Reckitt Benckiser LLC
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA021282
Marketing Category: NDA
Start Marketing Date: 20120626

Package Information of Mucinex

Package NDC: 63824-023-28
Package Description: 1 BOTTLE in 1 CARTON (63824-023-28) > 28 TABLET, EXTENDED RELEASE in 1 BOTTLE

NDC Information of Mucinex

NDC Code 63824-023-28
Proprietary Name Mucinex
Package Description 1 BOTTLE in 1 CARTON (63824-023-28) > 28 TABLET, EXTENDED RELEASE in 1 BOTTLE
Product NDC 63824-023
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Guaifenesin
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20120626
Marketing Category Name NDA
Labeler Name Reckitt Benckiser LLC
Substance Name GUAIFENESIN
Strength Number 1200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Mucinex


General Information