ADVAIR
- Product NDC
- 21695-361
- 11-digit product format
- 216950361
- Labeler code
- 21695
- Product ID
- 21695-361_0bfe9d76-1b0e-47a4-831d-097168d66577
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- fluticasone propionate and salmeterol
- Dosage form
- POWDER
- Route
- RESPIRATORY (INHALATION)
- Labeler
- Rebel Distributors Corp
- Application
- NDA021077
- Marketing category
- NDA
- Marketing start
- 2001-02-28
- Marketing end
- 0000-00-00
- Substance
- SALMETEROL XINAFOATE; FLUTICASONE PROPIONATE
- Active strength
- 50 ug/1; ug/1
- Pharmacologic classes
- Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 21695-361-60 | ADVAIRDISKUS | 60 in 1 INHALER | POWDER | 60 | 1 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 21695-361-60 | EA - Each | 21695-361 | 7ae69816-b36a-49a9-96bc-84d657daf70d | 1 | 2012-07-24 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| FLUTICASONE PROPIONATE | ACTIVE INGREDIENT | O2GMZ0LF5W | ADVAIR DISKUS (FLUTICASONE PROPIONATE AND SALMETEROL) POWDER [REBEL DISTRIBUTORS CORP] | 1 | |
| SALMETEROL XINAFOATE | ACTIVE INGREDIENT | 6EW8Q962A5 | ADVAIR DISKUS (FLUTICASONE PROPIONATE AND SALMETEROL) POWDER [REBEL DISTRIBUTORS CORP] | 1 | |
| FLUTICASONE | ACTIVE MOIETY | CUT2W21N7U | ADVAIR DISKUS (FLUTICASONE PROPIONATE AND SALMETEROL) POWDER [REBEL DISTRIBUTORS CORP] | 1 | |
| SALMETEROL | ACTIVE MOIETY | 2I4BC502BT | ADVAIR DISKUS (FLUTICASONE PROPIONATE AND SALMETEROL) POWDER [REBEL DISTRIBUTORS CORP] | 1 | |
| LACTOSE | INACTIVE INGREDIENT | J2B2A4N98G | ADVAIR DISKUS (FLUTICASONE PROPIONATE AND SALMETEROL) POWDER [REBEL DISTRIBUTORS CORP] | 1 |
DailyMed Dashboard NDC Coverage#
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 896185 | ADVAIR DISKUS 100/50 MCG/INHAL Dry Powder Inhaler, 60 Blisters | PSN | 0bfe9d76-1b0e-47a4-831d-097168d66577 | 1 |
| 896184 | fluticasone propionate/salmeterol 100/50 MCG/INHAL Dry Powder Inhaler, 60 Blisters | PSN | 0bfe9d76-1b0e-47a4-831d-097168d66577 | 1 |
| 896185 | 60 ACTUAT fluticasone propionate 0.1 MG/ACTUAT / salmeterol 0.05 MG/ACTUAT Dry Powder Inhaler [Advair] | SBD | 0bfe9d76-1b0e-47a4-831d-097168d66577 | 1 |
| 896184 | 60 ACTUAT fluticasone propionate 0.1 MG/ACTUAT / salmeterol 0.05 MG/ACTUAT Dry Powder Inhaler | SCD | 0bfe9d76-1b0e-47a4-831d-097168d66577 | 1 |
| 896185 | Advair Diskus 100/50 (fluticasone propionate 100 MCG / salmeterol 50 MCG (salmeterol xinafoate 72.5 MCG)) per ACTUAT Dry Powder Inhaler, 60 ACTUAT | SY | 0bfe9d76-1b0e-47a4-831d-097168d66577 | 1 |
| 896185 | Advair Diskus 100/50 Dry Powder Inhaler, 60 ACTUAT | SY | 0bfe9d76-1b0e-47a4-831d-097168d66577 | 1 |
| 896184 | fluticasone propionate 0.1 MG/ACTUAT / salmeterol 0.05 MG/ACTUAT Dry Powder Inhaler, 60 ACTUAT | SY | 0bfe9d76-1b0e-47a4-831d-097168d66577 | 1 |
| 896184 | fluticasone propionate 100 MCG / salmeterol 50 MCG (salmeterol xinafoate 72.5 MCG) per ACTUAT Dry Powder Inhaler, 60 ACTUAT | SY | 0bfe9d76-1b0e-47a4-831d-097168d66577 | 1 |
Packages#
| Package NDC | 11-digit format | Description | Status |
|---|---|---|---|
| 21695-361-60 | 21695036160 | 60 in 1 INHALER | Historical |