Nolix
- Product NDC
- 57893-311
- 11-digit product format
- 578930311
- Labeler code
- 57893
- Product ID
- 57893-311_dd036898-2d34-b977-e053-2a95a90aec6d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FLURANDRENOLIDE
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Artesa Labs, LLC
- Application
- ANDA205343
- Marketing category
- ANDA
- Marketing start
- 2017-05-22
- 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 |
|---|
| 57893-311-12 | 57893031112 | 120 mL in 1 BOTTLE (57893-311-12) | 120 ml | 2017-05-22 | 0000-00-00 | No | No | Current |