DESONATE
- Product NDC
- 50419-828
- 11-digit product format
- 504190828
- Labeler code
- 50419
- Product ID
- 50419-828_c13c4ae4-790e-43bf-9080-0a5bc6ec995b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- desonide
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Bayer HealthCare Pharmaceuticals Inc.
- Application
- NDA021844
- Marketing category
- NDA
- Marketing start
- 2006-10-20
- 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
- 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 |
|---|
| 50419-828-06 | 50419082806 | 1 TUBE in 1 CARTON (50419-828-06) > 60 g in 1 TUBE | 1 tube | 2019-07-23 | 0000-00-00 | No | No | Current |
| 50419-828-12 | 50419082812 | 2 TUBE in 1 CARTON (50419-828-12) > 60 g in 1 TUBE | 2 tube | 2019-07-23 | 0000-00-00 | No | No | Current |
| 50419-828-72 | 50419082872 | 1 TUBE in 1 CARTON (50419-828-72) > 3.5 g in 1 TUBE | 1 tube | 2019-07-23 | 0000-00-00 | No | No | Current |