Fluticasone Propionate
- Product NDC
- 76420-106
- 11-digit product format
- 764200106
- Labeler code
- 76420
- Product ID
- 76420-106_ead40f72-3d3e-1c2b-e053-2995a90ad35b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fluticasone Propionate
- Dosage form
- SPRAY, METERED
- Route
- NASAL
- Labeler
- Asclemed USA, Inc.
- Application
- ANDA077570
- Marketing category
- ANDA
- Marketing start
- 2008-01-16
- Substance
- FLUTICASONE PROPIONATE
- Active strength
- 50 ug/.1g
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 76420-106-16 | 76420010616 | 16 g in 1 BOTTLE, PUMP (76420-106-16) | 16 g | 2020-11-02 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Fluticasone Propionate | Asclemed USA, Inc. | ASCLEMED USA INC. DBA ENOVACHEM | 2022-10-12 | HUMAN PRESCRIPTION DRUG LABEL | 2 |