ADAPALENE
- Product NDC
- 82442-105
- 11-digit product format
- 824420105
- Labeler code
- 82442
- Product ID
- 82442-105_3e515a45-7c44-1e08-e063-6294a90a9621
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Adapalene
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Target Corporation
- Application
- ANDA215940
- Marketing category
- ANDA
- Marketing start
- 2024-07-19
- Substance
- ADAPALENE
- Active strength
- 1 mg/g
- Pharmacologic classes
- Retinoid [EPC], Retinoids [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data
- Finished product
- Yes
- Brand name base
- ADAPALENE
- Listing expiration
- 2026-12-31
Active Ingredients
| Ingredient | Strength |
|---|
| ADAPALENE | 1 mg/g |
Harmonized Identifiers
| Field | Values |
|---|
| Unii | 1L4806J2QF |
| Rxcui | 307731 |
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 1L4806J2QF | ADAPALENE | 106685-40-9 | ADAPALENE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 82442-105-01 | 82442010501 | 1 TUBE in 1 CARTON (82442-105-01) / 15 g in 1 TUBE | 1 tube | 2024-07-19 | No | No | Current |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| ADAPALENE | Target Corporation | Sun Pharma Canada Inc. | 2025-09-08 | HUMAN OTC DRUG LABEL | 4 |