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tussin dm max - 42507-799-34 - (Dextromethorphan HBr, Guaifenesin)

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Drug Information of tussin dm max

Product NDC: 42507-799
Proprietary Name: tussin dm max
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 tussin dm max

Product NDC: 42507-799
Labeler Name: HyVee Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100809

Package Information of tussin dm max

Package NDC: 42507-799-34
Package Description: 1 BOTTLE in 1 CARTON (42507-799-34) > 237 mL in 1 BOTTLE

NDC Information of tussin dm max

NDC Code 42507-799-34
Proprietary Name tussin dm max
Package Description 1 BOTTLE in 1 CARTON (42507-799-34) > 237 mL in 1 BOTTLE
Product NDC 42507-799
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Dextromethorphan HBr, Guaifenesin
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20100809
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name HyVee Inc
Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Strength Number 10; 200
Strength Unit mg/5mL; mg/5mL
Pharmaceutical Classes

Complete Information of tussin dm max


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