Tussin DM - 59779-557-34 - (Dextromethorphan HBr, Guaifenesin)

Alphabetical Index


Drug Information of Tussin DM

Product NDC: 59779-557
Proprietary Name: Tussin DM
Non Proprietary Name: Dextromethorphan HBr, Guaifenesin
Active Ingredient(s): 10; 200    mg/5mL; mg/5mL & nbsp;   Dextromethorphan HBr, Guaifenesin
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Tussin DM

Product NDC: 59779-557
Labeler Name: CVS Pharmacy
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100728

Package Information of Tussin DM

Package NDC: 59779-557-34
Package Description: 1 BOTTLE in 1 CARTON (59779-557-34) > 237 mL in 1 BOTTLE

NDC Information of Tussin DM

NDC Code 59779-557-34
Proprietary Name Tussin DM
Package Description 1 BOTTLE in 1 CARTON (59779-557-34) > 237 mL in 1 BOTTLE
Product NDC 59779-557
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Dextromethorphan HBr, Guaifenesin
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20100728
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name CVS Pharmacy
Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Strength Number 10; 200
Strength Unit mg/5mL; mg/5mL
Pharmaceutical Classes

Complete Information of Tussin DM


General Information