NDC 00173-696-00 - ADVAIR DISKUS
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 00173-696
- Requested NDC
- 00173-696-00
- Package NDCs from labels
- 00173-696-00
- Manufacturer
- Rebel Distributors Corp.
- Effective date
- 2010-09-01
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| ADVAIR DISKUS - Rebel Distributors Corp. | Rebel Distributors Corp. | 2010-09-01 | HUMAN PRESCRIPTION DRUG LABEL |
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 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.