DESRX
- Product NDC
- 44118-710
- 11-digit product format
- 441180710
- Labeler code
- 44118
- Product ID
- 44118-710_c10eb9ab-3a1c-793b-e053-2a95a90aa45e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DESONIDE
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Eckson Labs, LLC
- Application
- ANDA202470
- Marketing category
- ANDA
- Marketing start
- 2021-04-28
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 44118-710-60 | 44118071060 | 1 TUBE in 1 CARTON (44118-710-60) > 60 g in 1 TUBE | 1 tube | 2021-04-28 | 0000-00-00 | No | No | Current |