Mucinex DM - 63824-072-39 - (Guaifenesin and Dextromethorphan Hydrobromide)

Alphabetical Index


Drug Information of Mucinex DM

Product NDC: 63824-072
Proprietary Name: Mucinex DM
Non Proprietary Name: Guaifenesin and Dextromethorphan Hydrobromide
Active Ingredient(s): 60; 1200    mg/1; mg/1 & nbsp;   Guaifenesin and Dextromethorphan Hydrobromide
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Mucinex DM

Product NDC: 63824-072
Labeler Name: Reckitt Benckiser LLC
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA021620
Marketing Category: NDA
Start Marketing Date: 20120626

Package Information of Mucinex DM

Package NDC: 63824-072-39
Package Description: 1 BOTTLE in 1 BLISTER PACK (63824-072-39) > 38 TABLET, EXTENDED RELEASE in 1 BOTTLE

NDC Information of Mucinex DM

NDC Code 63824-072-39
Proprietary Name Mucinex DM
Package Description 1 BOTTLE in 1 BLISTER PACK (63824-072-39) > 38 TABLET, EXTENDED RELEASE in 1 BOTTLE
Product NDC 63824-072
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Guaifenesin and Dextromethorphan Hydrobromide
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20120626
Marketing Category Name NDA
Labeler Name Reckitt Benckiser LLC
Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Strength Number 60; 1200
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Mucinex DM


General Information