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Tussin DMMaximum Strength - 59779-967-04 - (Dextromethorphan HBr, Guaifenesin)

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Drug Information of Tussin DMMaximum Strength

Product NDC: 59779-967
Proprietary Name: Tussin DMMaximum Strength
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 DMMaximum Strength

Product NDC: 59779-967
Labeler Name: CVS Pharmacy
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20090701

Package Information of Tussin DMMaximum Strength

Package NDC: 59779-967-04
Package Description: 1 BOTTLE in 1 CARTON (59779-967-04) > 237 mL in 1 BOTTLE

NDC Information of Tussin DMMaximum Strength

NDC Code 59779-967-04
Proprietary Name Tussin DMMaximum Strength
Package Description 1 BOTTLE in 1 CARTON (59779-967-04) > 237 mL in 1 BOTTLE
Product NDC 59779-967
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Dextromethorphan HBr, Guaifenesin
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20090701
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name CVS Pharmacy
Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Strength Number 10; 200
Strength Unit mg/5mL; mg/5mL
Pharmaceutical Classes

Complete Information of Tussin DMMaximum Strength


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