wal tussin - 0363-0799-26 - (Dextromethorphan HBr, Guaifenesin)

Alphabetical Index


Drug Information of wal tussin

Product NDC: 0363-0799
Proprietary Name: wal tussin
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 wal tussin

Product NDC: 0363-0799
Labeler Name: Walgreen Company
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100126

Package Information of wal tussin

Package NDC: 0363-0799-26
Package Description: 1 BOTTLE in 1 CARTON (0363-0799-26) > 118 mL in 1 BOTTLE

NDC Information of wal tussin

NDC Code 0363-0799-26
Proprietary Name wal tussin
Package Description 1 BOTTLE in 1 CARTON (0363-0799-26) > 118 mL in 1 BOTTLE
Product NDC 0363-0799
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Dextromethorphan HBr, Guaifenesin
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20100126
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Walgreen Company
Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Strength Number 10; 200
Strength Unit mg/5mL; mg/5mL
Pharmaceutical Classes

Complete Information of wal tussin


General Information