Desonide
- Product NDC
- 68462-252
- 11-digit product format
- 684620252
- Labeler code
- 68462
- Product ID
- 68462-252_2652cc14-f89a-4d1a-abf4-afe6e3167190
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Desonide
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Glenmark Pharmaceuticals Inc., USA
- Application
- ANDA209729
- Marketing category
- ANDA
- Marketing start
- 2017-07-24
- Marketing end
- 2023-07-01
- Substance
- DESONIDE
- Active strength
- 1 mg/g
- 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 |
|---|
| 68462-252-17 | 68462025217 | 1 TUBE in 1 CARTON (68462-252-17) > 15 g in 1 TUBE | 1 tube | 2017-07-24 | 0000-00-00 | No | No | Current |
| 68462-252-65 | 68462025265 | 1 TUBE in 1 CARTON (68462-252-65) > 60 g in 1 TUBE | 1 tube | 2017-07-24 | 0000-00-00 | No | No | Current |