Fluticasone Propionate
- Product NDC
- 72189-004
- 11-digit product format
- 721890004
- Labeler code
- 72189
- Product ID
- 72189-004_4d3a96c7-d9d7-c351-e063-6394a90a680d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fluticasone Propionate
- Dosage form
- SPRAY, METERED
- Route
- NASAL
- Labeler
- Direct_RX
- Application
- ANDA077538
- Marketing category
- ANDA
- Marketing start
- 2019-06-18
- Substance
- FLUTICASONE PROPIONATE
- Active strength
- 50 ug/1
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Fluticasone Propionate
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| FLUTICASONE PROPIONATE | 50 ug/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | O2GMZ0LF5W |
| Rxcui | 1797907 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72189-004-01 | Fluticasone Propionate | 1 in 1 BOTTLE, SPRAY | SPRAY, METERED | 1 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72189-004 | FLUTICASONE PROPIONATE SPRAY, METERED [DIRECT_RX] | 2 | Current NDC, Legacy NDC, 1 package rows | 20250130_8b9f7474-8d89-b3e6-e053-2995a90aeddb.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72189-004-01 | 72189000401 | 1 SPRAY, METERED in 1 BOTTLE, SPRAY (72189-004-01) | 2019-06-18 | 0000-00-00 | No | No | Current |