Mucinex D - 63824-041-36 - (Guaifenesin and Pseudoephedrine Hydrochloride)

Alphabetical Index


Drug Information of Mucinex D

Product NDC: 63824-041
Proprietary Name: Mucinex D
Non Proprietary Name: Guaifenesin and Pseudoephedrine Hydrochloride
Active Ingredient(s): 1200; 120    mg/1; mg/1 & nbsp;   Guaifenesin and Pseudoephedrine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Mucinex D

Product NDC: 63824-041
Labeler Name: Reckitt Benckiser LLC
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA021585
Marketing Category: NDA
Start Marketing Date: 20120626

Package Information of Mucinex D

Package NDC: 63824-041-36
Package Description: 3 BLISTER PACK in 1 CARTON (63824-041-36) > 12 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

NDC Information of Mucinex D

NDC Code 63824-041-36
Proprietary Name Mucinex D
Package Description 3 BLISTER PACK in 1 CARTON (63824-041-36) > 12 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC 63824-041
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Guaifenesin and Pseudoephedrine Hydrochloride
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; PSEUDOEPHEDRINE HYDROCHLORIDE
Strength Number 1200; 120
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Mucinex D


General Information