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