Flurandrenolide
- Product NDC
- 72162-1439
- 11-digit product format
- 721621439
- Labeler code
- 72162
- Product ID
- 72162-1439_f3f324b5-23ff-4171-b94f-db557655691b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Flurandrenolide
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA207133
- Marketing category
- ANDA
- Marketing start
- 2016-10-06
- Substance
- FLURANDRENOLIDE
- Active strength
- .5 mg/mL
- 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 |
|---|
| 8EUL29XUQT | FLURANDRENOLIDE | 1524-88-5 | FLURANDRENOLIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-1439-2 | 72162143902 | 120 mL in 1 BOTTLE (72162-1439-2) | 120 ml | 2023-08-17 | No | No | Historical |