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ADVAIRDISKUS - 49349-738-01 - (fluticasone propionate and salmeterol)

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Drug Information of ADVAIRDISKUS

Product NDC: 49349-738
Proprietary Name: ADVAIRDISKUS
Non Proprietary Name: fluticasone propionate and salmeterol
Active Ingredient(s): 500; 50    ug/1; ug/1 & nbsp;   fluticasone propionate and salmeterol
Administration Route(s): RESPIRATORY (INHALATION)
Dosage Form(s): POWDER
Coding System: National Drug Codes(NDC)

Labeler Information of ADVAIRDISKUS

Product NDC: 49349-738
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021077
Marketing Category: NDA
Start Marketing Date: 20130610

Package Information of ADVAIRDISKUS

Package NDC: 49349-738-01
Package Description: 60 POWDER in 1 INHALER (49349-738-01)

NDC Information of ADVAIRDISKUS

NDC Code 49349-738-01
Proprietary Name ADVAIRDISKUS
Package Description 60 POWDER in 1 INHALER (49349-738-01)
Product NDC 49349-738
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fluticasone propionate and salmeterol
Dosage Form Name POWDER
Route Name RESPIRATORY (INHALATION)
Start Marketing Date 20130610
Marketing Category Name NDA
Labeler Name REMEDYREPACK INC.
Substance Name FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE
Strength Number 500; 50
Strength Unit ug/1; ug/1
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA],Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC]

Complete Information of ADVAIRDISKUS


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