Wal Tussin - 0363-0359-34 - (Dextromethorphan Hydrobromide, Guaifenesin)

Alphabetical Index


Drug Information of Wal Tussin

Product NDC: 0363-0359
Proprietary Name: Wal Tussin
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 Wal Tussin

Product NDC: 0363-0359
Labeler Name: Walgreen Company
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19951006

Package Information of Wal Tussin

Package NDC: 0363-0359-34
Package Description: 1 BOTTLE in 1 CARTON (0363-0359-34) > 237 mL in 1 BOTTLE

NDC Information of Wal Tussin

NDC Code 0363-0359-34
Proprietary Name Wal Tussin
Package Description 1 BOTTLE in 1 CARTON (0363-0359-34) > 237 mL in 1 BOTTLE
Product NDC 0363-0359
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Dextromethorphan Hydrobromide, Guaifenesin
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 19951006
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Walgreen Company
Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Strength Number 10; 100
Strength Unit mg/5mL; mg/5mL
Pharmaceutical Classes

Complete Information of Wal Tussin


General Information