Fluticasone Propionate
- Product NDC
- 76420-329
- 11-digit product format
- 764200329
- Labeler code
- 76420
- Product ID
- 76420-329_331b68c0-b022-b6c8-e063-6394a90aa819
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fluticasone Propionate
- Dosage form
- SPRAY, METERED
- Route
- NASAL
- Labeler
- Asclemed USA, Inc.
- Application
- ANDA076504
- Marketing category
- ANDA
- Marketing start
- 2006-02-22
- Substance
- FLUTICASONE PROPIONATE
- Active strength
- 50 ug/1
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| O2GMZ0LF5W | FLUTICASONE PROPIONATE | 80474-14-2 | FLUTICASONE PROPIONATE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 76420-329-50 | 76420032950 | 1 BOTTLE, GLASS in 1 CARTON (76420-329-50) / 120 SPRAY, METERED in 1 BOTTLE, GLASS | 2025-04-19 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Fluticasone Propionate | Asclemed USA, Inc. | ASCLEMED USA INC. DBA ENOVACHEM | 2025-04-19 | HUMAN PRESCRIPTION DRUG LABEL | 1 |