Flurandrenolide
- Product NDC
- 72162-1439
- 11-digit product format
- 721621439
- Labeler code
- 72162
- Product ID
- 72162-1439_f3f324b5-23ff-4171-b94f-db557655691b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Flurandrenolide
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA207133
- Marketing category
- ANDA
- Marketing start
- 2016-10-06
- Substance
- FLURANDRENOLIDE
- Active strength
- .5 mg/mL
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Flurandrenolide
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| FLURANDRENOLIDE | .5 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 8EUL29XUQT |
| Rxcui | 197719 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-1439-2 | Flurandrenolide | 120 mL in 1 BOTTLE | LOTION | 120 | | 100 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-1439 | FLURANDRENOLIDE LOTION [BRYANT RANCH PREPACK] | 100 | Current NDC, 1 package rows | 20230824_2718df54-7dc1-4ebc-8258-607bedcf5813.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 |
|---|
| 72162-1439-2 | 72162143902 | 120 mL in 1 BOTTLE (72162-1439-2) | 120 ml | 2023-08-17 | No | No | Current |