FLUTICASONE PROPIONATE
- Product NDC
- 68071-3949
- 11-digit product format
- 680713949
- Labeler code
- 68071
- Product ID
- 68071-3949_4849c4ec-c391-912e-e063-6394a90a1c24
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FLUTICASONE PROPIONATE
- Dosage form
- SPRAY
- Route
- NASAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA218321
- Marketing category
- ANDA
- Marketing start
- 2025-06-05
- 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 |
|---|
| 68071-3949-5 | FLUTICASONE PROPIONATE | 1 in 1 CARTON | SPRAY | 1 | | 1 |
| 68071-3949-5 | FLUTICASONE PROPIONATE | 120 in 1 BOTTLE, SPRAY | SPRAY | 120 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 68071-3949-5 | 68071394905 | 1 BOTTLE, SPRAY in 1 CARTON (68071-3949-5) / 120 SPRAY in 1 BOTTLE, SPRAY | 2026-01-13 | No | No | Historical |