Tussin DM - 37808-359-40 - (Dextromethorphan Hydrobromide, Guaifenesin)

Alphabetical Index


Drug Information of Tussin DM

Product NDC: 37808-359
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: 37808-359
Labeler Name: H E B
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19910809

Package Information of Tussin DM

Package NDC: 37808-359-40
Package Description: 1 BOTTLE in 1 CARTON (37808-359-40) > 355 mL in 1 BOTTLE

NDC Information of Tussin DM

NDC Code 37808-359-40
Proprietary Name Tussin DM
Package Description 1 BOTTLE in 1 CARTON (37808-359-40) > 355 mL in 1 BOTTLE
Product NDC 37808-359
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Dextromethorphan Hydrobromide, Guaifenesin
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 19910809
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name H E B
Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Strength Number 10; 100
Strength Unit mg/5mL; mg/5mL
Pharmaceutical Classes

Complete Information of Tussin DM


General Information