Desonide
- Product NDC
- 71589-005
- 11-digit product format
- 715890005
- Labeler code
- 71589
- Product ID
- 71589-005_8ea5fc2d-29ab-4c7b-b7be-3c4b86bc3f73
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Desonide
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Aleor Dermaceuticals Limited
- Application
- ANDA212473
- Marketing category
- ANDA
- Marketing start
- 2019-11-02
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71589-005-15 | 71589000515 | 1 TUBE in 1 CARTON (71589-005-15) > 15 g in 1 TUBE | 1 tube | 2019-11-02 | 0000-00-00 | No | No | Current |
| 71589-005-60 | 71589000560 | 1 TUBE in 1 CARTON (71589-005-60) > 60 g in 1 TUBE | 1 tube | 2019-11-02 | 0000-00-00 | No | No | Current |