ADVAIR - 21695-197-01 - (fluticasone propionate and salmeterol)

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Drug Information of ADVAIR

Product NDC: 21695-197
Proprietary Name: ADVAIR
Non Proprietary Name: fluticasone propionate and salmeterol
Active Ingredient(s): 500; 50    ug/1; ug/1 & nbsp;   fluticasone propionate and salmeterol
Administration Route(s): ORAL; RESPIRATORY (INHALATION)
Dosage Form(s): POWDER
Coding System: National Drug Codes(NDC)

Labeler Information of ADVAIR

Product NDC: 21695-197
Labeler Name: Rebel Distributors Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021077
Marketing Category: NDA
Start Marketing Date: 20010305

Package Information of ADVAIR

Package NDC: 21695-197-01
Package Description: 60 POWDER in 1 INHALER (21695-197-01)

NDC Information of ADVAIR

NDC Code 21695-197-01
Proprietary Name ADVAIR
Package Description 60 POWDER in 1 INHALER (21695-197-01)
Product NDC 21695-197
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fluticasone propionate and salmeterol
Dosage Form Name POWDER
Route Name ORAL; RESPIRATORY (INHALATION)
Start Marketing Date 20010305
Marketing Category Name NDA
Labeler Name Rebel Distributors Corp.
Substance Name FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE
Strength Number 500; 50
Strength Unit ug/1; ug/1
Pharmaceutical Classes Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of ADVAIR


General Information