Tussin - 68016-020-04 - (GUAIFENESIN)

Alphabetical Index


Drug Information of Tussin

Product NDC: 68016-020
Proprietary Name: Tussin
Non Proprietary Name: GUAIFENESIN
Active Ingredient(s): 100    mg/5mL & nbsp;   GUAIFENESIN
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Tussin

Product NDC: 68016-020
Labeler Name: Chain Drug Consortium, LLC
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120907

Package Information of Tussin

Package NDC: 68016-020-04
Package Description: 118 mL in 1 BOTTLE, PLASTIC (68016-020-04)

NDC Information of Tussin

NDC Code 68016-020-04
Proprietary Name Tussin
Package Description 118 mL in 1 BOTTLE, PLASTIC (68016-020-04)
Product NDC 68016-020
Product Type Name HUMAN OTC DRUG
Non Proprietary Name GUAIFENESIN
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20120907
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Chain Drug Consortium, LLC
Substance Name GUAIFENESIN
Strength Number 100
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of Tussin


General Information