tussin - 55312-359-26 - (Dextromethorphan HBr, Guaifenesin)

Alphabetical Index


Drug Information of tussin

Product NDC: 55312-359
Proprietary Name: tussin
Non Proprietary Name: Dextromethorphan HBr, Guaifenesin
Active Ingredient(s): 10; 100    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 tussin

Product NDC: 55312-359
Labeler Name: Western Family Foods Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19910809

Package Information of tussin

Package NDC: 55312-359-26
Package Description: 1 BOTTLE in 1 CARTON (55312-359-26) > 118 mL in 1 BOTTLE

NDC Information of tussin

NDC Code 55312-359-26
Proprietary Name tussin
Package Description 1 BOTTLE in 1 CARTON (55312-359-26) > 118 mL in 1 BOTTLE
Product NDC 55312-359
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Dextromethorphan HBr, Guaifenesin
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 19910809
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Western Family Foods Inc
Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Strength Number 10; 100
Strength Unit mg/5mL; mg/5mL
Pharmaceutical Classes

Complete Information of tussin


General Information