Tussin DM - 70253-018-04 - (Dextromethorphan Hydrobromide, Guaifenesin)

Alphabetical Index


Drug Information of Tussin DM

Product NDC: 70253-018
Proprietary Name: Tussin DM
Non Proprietary Name: Dextromethorphan Hydrobromide, Guaifenesin
Active Ingredient(s): 10; 100    mg/5mL; mg/5mL & nbsp;   Dextromethorphan Hydrobromide, Guaifenesin
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Tussin DM

Product NDC: 70253-018
Labeler Name: Nash-Finch Company
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20090603

Package Information of Tussin DM

Package NDC: 70253-018-04
Package Description: 118 mL in 1 BOTTLE, PLASTIC (70253-018-04)

NDC Information of Tussin DM

NDC Code 70253-018-04
Proprietary Name Tussin DM
Package Description 118 mL in 1 BOTTLE, PLASTIC (70253-018-04)
Product NDC 70253-018
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Dextromethorphan Hydrobromide, Guaifenesin
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20090603
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Nash-Finch Company
Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Strength Number 10; 100
Strength Unit mg/5mL; mg/5mL
Pharmaceutical Classes

Complete Information of Tussin DM


General Information