Fluticasone Propionate
- Product NDC
- 70518-0880
- 11-digit product format
- 705180880
- Labeler code
- 70518
- Product ID
- 70518-0880_4846e8db-8881-525f-e063-6394a90a7415
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fluticasone Propionate
- Dosage form
- SPRAY, METERED
- Route
- NASAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA076504
- Marketing category
- ANDA
- Marketing start
- 2018-03-15
- 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#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-0880-0 | Fluticasone Propionate | 1 in 1 CARTON | SPRAY, METERED | 1 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-0880 | FLUTICASONE PROPIONATE SPRAY, METERED [REMEDYREPACK INC.] | 4 | Current NDC, Legacy NDC, 1 package rows | 20250523_3c7e3ae6-a78f-4023-a2d4-543615ae25b0.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 70518-0880-0 | 70518088000 | 1 SPRAY, METERED in 1 CARTON (70518-0880-0) | 2018-03-15 | No | No | Current |