Flurandrenolide
- Product NDC
- 24470-921
- 11-digit product format
- 244700921
- Labeler code
- 24470
- Product ID
- 24470-921_dd0374f4-9f04-58cf-e053-2995a90a2f7e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FLURANDRENOLIDE
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Cintex Services, LLC
- Application
- ANDA205343
- Marketing category
- ANDA
- Marketing start
- 2016-12-22
- Marketing end
- 2022-06-30
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 24470-921-12 | 24470092112 | 120 mL in 1 BOTTLE (24470-921-12) | 120 ml | 2016-12-22 | 0000-00-00 | No | No | Current |
| 24470-921-60 | 24470092160 | 60 mL in 1 BOTTLE (24470-921-60) | 60 ml | 2016-12-22 | 0000-00-00 | No | No | Current |