Desonide
- Product NDC
- 68462-528
- 11-digit product format
- 684620528
- Labeler code
- 68462
- Product ID
- 68462-528_65801eb0-739a-4c13-88b3-786ad5110edd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Desonide
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Glenmark Pharmaceuticals Inc., USA
- Application
- ANDA209996
- Marketing category
- ANDA
- Marketing start
- 2017-09-15
- Marketing end
- 2023-02-01
- Substance
- DESONIDE
- Active strength
- 1 mg/g
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- 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 |
|---|
| 68462-528-17 | 68462052817 | 1 TUBE in 1 CARTON (68462-528-17) > 15 g in 1 TUBE | 1 tube | 2017-09-15 | 2022-12-01 | No | No | Current |
| 68462-528-65 | 68462052865 | 1 TUBE in 1 CARTON (68462-528-65) > 60 g in 1 TUBE | 1 tube | 2017-09-15 | 2023-02-01 | No | No | Current |