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Mucus Relief DM - 0904-6013-14 - (Dextromethorphan HBr and Guiafenesin)

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Drug Information of Mucus Relief DM

Product NDC: 0904-6013
Proprietary Name: Mucus Relief DM
Non Proprietary Name: Dextromethorphan HBr and Guiafenesin
Active Ingredient(s): 20; 400    mg/1; mg/1 & nbsp;   Dextromethorphan HBr and Guiafenesin
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Mucus Relief DM

Product NDC: 0904-6013
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20051231

Package Information of Mucus Relief DM

Package NDC: 0904-6013-14
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0904-6013-14)

NDC Information of Mucus Relief DM

NDC Code 0904-6013-14
Proprietary Name Mucus Relief DM
Package Description 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0904-6013-14)
Product NDC 0904-6013
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Dextromethorphan HBr and Guiafenesin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20051231
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Major Pharmaceuticals
Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Strength Number 20; 400
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Mucus Relief DM


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