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Mucus Relief D - 41250-547-72 - (Guaifenesin, Pseudoephedrine HCl)

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Drug Information of Mucus Relief D

Product NDC: 41250-547
Proprietary Name: Mucus Relief D
Non Proprietary Name: Guaifenesin, Pseudoephedrine HCl
Active Ingredient(s): 400; 40    mg/1; mg/1 & nbsp;   Guaifenesin, Pseudoephedrine HCl
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Mucus Relief D

Product NDC: 41250-547
Labeler Name: Meijer
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20070126

Package Information of Mucus Relief D

Package NDC: 41250-547-72
Package Description: 3 BLISTER PACK in 1 CARTON (41250-547-72) > 9 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Mucus Relief D

NDC Code 41250-547-72
Proprietary Name Mucus Relief D
Package Description 3 BLISTER PACK in 1 CARTON (41250-547-72) > 9 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 41250-547
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Guaifenesin, Pseudoephedrine HCl
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070126
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Meijer
Substance Name GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE
Strength Number 400; 40
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Mucus Relief D


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