Desonide
- Product NDC
- 61748-470
- 11-digit product format
- 617480470
- Labeler code
- 61748
- Product ID
- 61748-470_049acd34-72d3-408a-b321-56d58db9d720
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Desonide
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Versapharm Incorporated
- Application
- ANDA208836
- Marketing category
- ANDA
- Marketing start
- 2017-09-01
- 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
- 2021-12-31
- 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 |
|---|
| 61748-470-15 | 61748047015 | 1 TUBE in 1 CARTON (61748-470-15) > 15 g in 1 TUBE | 1 tube | 2017-09-01 | 0000-00-00 | No | No | Current |
| 61748-470-60 | 61748047060 | 1 TUBE in 1 CARTON (61748-470-60) > 60 g in 1 TUBE | 1 tube | 2017-09-01 | 0000-00-00 | No | No | Current |