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Equaline tussin - 41163-359-34 - (Dextromethorphan HBr, Guaifenesin)

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Drug Information of Equaline tussin

Product NDC: 41163-359
Proprietary Name: Equaline 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 Equaline tussin

Product NDC: 41163-359
Labeler Name: Supervalu Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20040824

Package Information of Equaline tussin

Package NDC: 41163-359-34
Package Description: 1 BOTTLE in 1 CARTON (41163-359-34) > 237 mL in 1 BOTTLE

NDC Information of Equaline tussin

NDC Code 41163-359-34
Proprietary Name Equaline tussin
Package Description 1 BOTTLE in 1 CARTON (41163-359-34) > 237 mL in 1 BOTTLE
Product NDC 41163-359
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Dextromethorphan HBr, Guaifenesin
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20040824
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Supervalu Inc
Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Strength Number 10; 100
Strength Unit mg/5mL; mg/5mL
Pharmaceutical Classes

Complete Information of Equaline tussin


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