Desonide
- Product NDC
- 70710-1235
- 11-digit product format
- 707101235
- Labeler code
- 70710
- Product ID
- 70710-1235_95efe78a-806f-4102-be79-c7827662cfad
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Desonide
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Zydus Pharmaceuticals (USA) Inc.
- Application
- ANDA210198
- Marketing category
- ANDA
- Marketing start
- 2019-11-25
- Marketing end
- 2022-01-31
- Substance
- DESONIDE
- Active strength
- 1 mg/g
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- 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 |
|---|
| 70710-1235-1 | 70710123501 | 1 TUBE in 1 CARTON (70710-1235-1) > 15 g in 1 TUBE | 1 tube | 2019-11-25 | 0000-00-00 | No | No | Current |
| 70710-1235-3 | 70710123503 | 1 TUBE in 1 CARTON (70710-1235-3) > 60 g in 1 TUBE | 1 tube | 2019-11-25 | 0000-00-00 | No | No | Current |