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Mucus Relief - 50844-532-11 - (Guaifenesin)

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Drug Information of Mucus Relief

Product NDC: 50844-532
Proprietary Name: Mucus Relief
Non Proprietary Name: Guaifenesin
Active Ingredient(s): 400    mg/1 & nbsp;   Guaifenesin
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Mucus Relief

Product NDC: 50844-532
Labeler Name: L.N.K. International, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19951222

Package Information of Mucus Relief

Package NDC: 50844-532-11
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (50844-532-11) > 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

NDC Information of Mucus Relief

NDC Code 50844-532-11
Proprietary Name Mucus Relief
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (50844-532-11) > 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product NDC 50844-532
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Guaifenesin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19951222
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name L.N.K. International, Inc.
Substance Name GUAIFENESIN
Strength Number 400
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Mucus Relief


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