Fluticasone
- Product NDC
- 50436-2640
- 11-digit product format
- 504362640
- Labeler code
- 50436
- Product ID
- 50436-2640_015b035a-00e5-45d0-9b3b-9de18a3be561
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fluticasone Propionate
- Dosage form
- SPRAY, METERED
- Route
- NASAL
- Labeler
- Unit Dose Services
- Application
- ANDA078492
- Marketing category
- ANDA
- Marketing start
- 2012-01-09
- Marketing end
- 0000-00-00
- Substance
- FLUTICASONE PROPIONATE
- Active strength
- 50 ug/1
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50436-2640-1 | Fluticasone | 120 in 1 BOTTLE, SPRAY | SPRAY, METERED | 120 | | 5 |
| 50436-2640-1 | Fluticasone | 1 in 1 BOX | SPRAY, METERED | 1 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-2640 | FLUTICASONE (FLUTICASONE PROPIONATE) SPRAY, METERED [UNIT DOSE SERVICES] | 5 | Legacy NDC, 2 package rows | 20170307_21542935-c111-45f2-a0a5-62656ea6d843.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50436-2640-1 | 50436264001 | 120 in 1 BOTTLE, SPRAY | Historical |