desonide
- Product NDC
- 68462-513
- 11-digit product format
- 684620513
- Labeler code
- 68462
- Product ID
- 68462-513_8b6778b3-3c45-4d69-925f-d4876398fabe
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- desonide
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Glenmark Pharmaceuticals Inc., USA
- Application
- ANDA209494
- Marketing category
- ANDA
- Marketing start
- 2017-09-26
- Marketing end
- 2023-05-01
- Substance
- DESONIDE
- Active strength
- 1 mg/mL
- 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 |
|---|
| 68462-513-39 | 68462051339 | 1 BOTTLE in 1 CARTON (68462-513-39) > 59 mL in 1 BOTTLE | 1 bottle | 2017-09-26 | 0000-00-00 | No | No | Current |
| 68462-513-89 | 68462051389 | 1 BOTTLE in 1 CARTON (68462-513-89) > 118 mL in 1 BOTTLE | 1 bottle | 2017-09-26 | 0000-00-00 | No | No | Current |