DESONIDE
- Product NDC
- 52187-556
- 11-digit product format
- 521870556
- Labeler code
- 52187
- Product ID
- 52187-556_df7434aa-d4bf-63a1-e053-2a95a90a2751
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DESONIDE
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- KMM Pharmaceuticals, LLC
- Application
- ANDA202470
- Marketing category
- ANDA
- Marketing start
- 2022-02-28
- Marketing end
- 0000-00-00
- Substance
- DESONIDE
- Active strength
- 1 mg/g
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 52187-556-60 | 52187055660 | 1 TUBE in 1 CARTON (52187-556-60) > 60 g in 1 TUBE | 1 tube | 2022-02-28 | 0000-00-00 | No | No | Current |