Fluticasone Propionate
- Product NDC
- 0168-0333
- 11-digit product format
- 001680333
- Labeler code
- 0168
- Product ID
- 0168-0333_7bc876cd-707f-4206-a612-c04b370b41c5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- fluticasone propionate
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- E. Fougera & Co. a division of Fougera Pharmaceuticals Inc.
- Application
- ANDA076300
- Marketing category
- ANDA
- Marketing start
- 2004-05-14
- Marketing end
- 0000-00-00
- Substance
- FLUTICASONE PROPIONATE
- Active strength
- 0 mg/g
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0168-0333-15 | 00168033315 | 15 g in 1 TUBE (0168-0333-15) | 15 g | 2004-05-14 | 0000-00-00 | No | No | Current |
| 0168-0333-30 | 00168033330 | 30 g in 1 TUBE (0168-0333-30) | 30 g | 2004-05-14 | 0000-00-00 | No | No | Current |
| 0168-0333-60 | 00168033360 | 60 g in 1 TUBE (0168-0333-60) | 60 g | 2004-05-14 | 0000-00-00 | No | No | Current |