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MUCUS RELIEF DM - 0904-6233-52 - (GUAIFENESIN, DEXTROMETHORPHAN HBr)

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Drug Information of MUCUS RELIEF DM

Product NDC: 0904-6233
Proprietary Name: MUCUS RELIEF DM
Non Proprietary Name: GUAIFENESIN, DEXTROMETHORPHAN HBr
Active Ingredient(s): 20; 400    mg/1; mg/1 & nbsp;   GUAIFENESIN, DEXTROMETHORPHAN HBr
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of MUCUS RELIEF DM

Product NDC: 0904-6233
Labeler Name: MAJOR PHARMACEUTICALS INC
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120723

Package Information of MUCUS RELIEF DM

Package NDC: 0904-6233-52
Package Description: 60 TABLET in 1 BOTTLE, PLASTIC (0904-6233-52)

NDC Information of MUCUS RELIEF DM

NDC Code 0904-6233-52
Proprietary Name MUCUS RELIEF DM
Package Description 60 TABLET in 1 BOTTLE, PLASTIC (0904-6233-52)
Product NDC 0904-6233
Product Type Name HUMAN OTC DRUG
Non Proprietary Name GUAIFENESIN, DEXTROMETHORPHAN HBr
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120723
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name MAJOR PHARMACEUTICALS INC
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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