Flurandrenolide
- Product NDC
- 51672-5298
- 11-digit product format
- 516725298
- Labeler code
- 51672
- Product ID
- 51672-5298_6f5bce42-23d5-4698-ab11-070e3a6be2c7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Flurandrenolide
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Taro Pharmaceuticals U.S.A., Inc.
- Application
- NDA013790
- Marketing category
- NDA
- Marketing start
- 2016-04-25
- Marketing end
- 2022-09-30
- Substance
- FLURANDRENOLIDE
- Active strength
- 1 mg/mL
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51672-5298-8 | 51672529808 | 1 BOTTLE, PLASTIC in 1 CARTON (51672-5298-8) > 120 mL in 1 BOTTLE, PLASTIC | 2016-04-25 | 2022-09-30 | No | No | Current |