Tusnel - 54859-502-06 - (Dextromethorphan, Guiafenesin, Pseudoephedrine HCl)

Alphabetical Index


Drug Information of Tusnel

Product NDC: 54859-502
Proprietary Name: Tusnel
Non Proprietary Name: Dextromethorphan, Guiafenesin, Pseudoephedrine HCl
Active Ingredient(s): 15; 200; 30    mg/5mL; mg/5mL; mg/5mL & nbsp;   Dextromethorphan, Guiafenesin, Pseudoephedrine HCl
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Tusnel

Product NDC: 54859-502
Labeler Name: Llorens Pharmaceutical International Division
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20060101

Package Information of Tusnel

Package NDC: 54859-502-06
Package Description: 178 mL in 1 BOTTLE (54859-502-06)

NDC Information of Tusnel

NDC Code 54859-502-06
Proprietary Name Tusnel
Package Description 178 mL in 1 BOTTLE (54859-502-06)
Product NDC 54859-502
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Dextromethorphan, Guiafenesin, Pseudoephedrine HCl
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20060101
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Llorens Pharmaceutical International Division
Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE
Strength Number 15; 200; 30
Strength Unit mg/5mL; mg/5mL; mg/5mL
Pharmaceutical Classes

Complete Information of Tusnel


General Information