DESONIDE
- Product NDC
- 57893-317
- 11-digit product format
- 578930317
- Labeler code
- 57893
- Product ID
- 57893-317_bc1d06ae-ba74-49dc-e053-2995a90aacbe
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Desonide
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Artesa Labs, LLC
- Application
- ANDA202470
- Marketing category
- ANDA
- Marketing start
- 2021-02-24
- Marketing end
- 0000-00-00
- Substance
- DESONIDE
- Active strength
- 1 mg/g
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 57893-317-60 | 57893031760 | 1 TUBE in 1 CARTON (57893-317-60) > 60 g in 1 TUBE | 1 tube | 2021-02-24 | 0000-00-00 | No | No | Current |