Desonide
- Product NDC
- 72162-2005
- 11-digit product format
- 721622005
- Labeler code
- 72162
- Product ID
- 72162-2005_a0792f7b-faeb-475d-a030-ef46e876c2d0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Desonide
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA210198
- Marketing category
- ANDA
- Marketing start
- 2020-06-17
- Substance
- DESONIDE
- Active strength
- .5 mg/g
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Desonide
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DESONIDE | .5 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | J280872D1O |
| Rxcui | 349351 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-2005 | DESONIDE CREAM [BRYANT RANCH PREPACK] | 100 | Current NDC, 4 package rows | 20240201_217e953b-4296-4c5a-ae07-675c96c35249.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2005-2 | 72162200502 | 1 TUBE in 1 CARTON (72162-2005-2) / 15 g in 1 TUBE | 1 tube | 2020-06-17 | No | No | Current |
| 72162-2005-6 | 72162200506 | 1 TUBE in 1 CARTON (72162-2005-6) / 60 g in 1 TUBE | 1 tube | 2020-06-17 | No | No | Current |