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tussin cough dm - 41268-359-34 - (Dextromethorphan Hydrobromide, Guaifenesin)

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Drug Information of tussin cough dm

Product NDC: 41268-359
Proprietary Name: tussin cough dm
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 tussin cough dm

Product NDC: 41268-359
Labeler Name: Hannaford Brothers Company
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19950809

Package Information of tussin cough dm

Package NDC: 41268-359-34
Package Description: 1 BOTTLE in 1 CARTON (41268-359-34) > 237 mL in 1 BOTTLE

NDC Information of tussin cough dm

NDC Code 41268-359-34
Proprietary Name tussin cough dm
Package Description 1 BOTTLE in 1 CARTON (41268-359-34) > 237 mL in 1 BOTTLE
Product NDC 41268-359
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Dextromethorphan Hydrobromide, Guaifenesin
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 19950809
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Hannaford Brothers Company
Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Strength Number 10; 100
Strength Unit mg/5mL; mg/5mL
Pharmaceutical Classes

Complete Information of tussin cough dm


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