flurandrenolide
- Product NDC
- 51862-158
- 11-digit product format
- 518620158
- Labeler code
- 51862
- Product ID
- 51862-158_92e4f6bf-4c4a-4a8e-92a7-830c37df3785
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- flurandrenolide
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Mayne Pharma Inc.
- Application
- ANDA207851
- Marketing category
- ANDA
- Marketing start
- 2019-11-29
- Marketing end
- 0000-00-00
- Substance
- FLURANDRENOLIDE
- Active strength
- 1 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 |
|---|
| 51862-158-60 | 51862015860 | 1 TUBE in 1 CARTON (51862-158-60) > 60 g in 1 TUBE | 1 tube | 2019-11-29 | 0000-00-00 | No | No | Current |