Fluticasone Propionate
- Product NDC
- 53002-7692
- 11-digit product format
- 530027692
- Labeler code
- 53002
- Product ID
- 53002-7692_13f45c59-897e-4f4f-a3c9-d2068151c2bf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fluticasone Propionate
- Dosage form
- SPRAY, METERED
- Route
- NASAL
- Labeler
- RPK Pharmaceuticals, Inc.
- Application
- ANDA077570
- Marketing category
- ANDA
- Marketing start
- 2008-01-16
- Marketing end
- 0000-00-00
- Substance
- FLUTICASONE PROPIONATE
- Active strength
- 50 ug/.1g
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 53002-7692-1 | 53002769201 | 1 BOTTLE, PUMP in 1 CARTON (53002-7692-1) > 16 g in 1 BOTTLE, PUMP | 2020-01-01 | 0000-00-00 | No | No | Current |