Mucinex - 17856-0008-2 - (Guaifenesin)

Alphabetical Index


Drug Information of Mucinex

Product NDC: 17856-0008
Proprietary Name: Mucinex
Non Proprietary Name: Guaifenesin
Active Ingredient(s): 600    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: 17856-0008
Labeler Name: Atlantic Biologicals Corps
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA021282
Marketing Category: NDA
Start Marketing Date: 20120703

Package Information of Mucinex

Package NDC: 17856-0008-2
Package Description: 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (17856-0008-2)

NDC Information of Mucinex

NDC Code 17856-0008-2
Proprietary Name Mucinex
Package Description 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (17856-0008-2)
Product NDC 17856-0008
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Guaifenesin
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20120703
Marketing Category Name NDA
Labeler Name Atlantic Biologicals Corps
Substance Name GUAIFENESIN
Strength Number 600
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Mucinex


General Information