Desonide
- Product NDC
- 16714-828
- 11-digit product format
- 167140828
- Labeler code
- 16714
- Product ID
- 16714-828_f7d45cbe-363d-4b2d-bef5-f2cc0f7da813
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Desonide
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Northstar Rx LLC
- Application
- ANDA209996
- Marketing category
- ANDA
- Marketing start
- 2017-09-15
- 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 |
|---|
| 16714-828-01 | 16714082801 | 1 TUBE in 1 CARTON (16714-828-01) > 15 g in 1 TUBE | 1 tube | 2018-07-16 | 0000-00-00 | No | No | Current |
| 16714-828-02 | 16714082802 | 1 TUBE in 1 CARTON (16714-828-02) > 60 g in 1 TUBE | 1 tube | 2018-07-16 | 0000-00-00 | No | No | Current |