Fluocinonide
- Product NDC
- 72162-1972
- 11-digit product format
- 721621972
- Labeler code
- 72162
- Product ID
- 72162-1972_5edcc198-5b9e-4867-a853-4844fbf5c919
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fluocinonide
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA212976
- Marketing category
- ANDA
- Marketing start
- 2019-12-09
- Substance
- FLUOCINONIDE
- Active strength
- .05 mg/g
- 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
- Fluocinonide
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| FLUOCINONIDE | .05 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 2W4A77YPAN |
DailyMed Product Concepts#
DailyMed Package Descriptions#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-1972 | FLUOCINONIDE (FLUOCINONIDE ) OINTMENT [BRYANT RANCH PREPACK] | 100 | Current NDC, 6 package rows | 20240203_9bad56f2-6070-44fc-a39d-bb00280057f0.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-1972-2 | 72162197202 | 1 TUBE in 1 CARTON (72162-1972-2) / 15 g in 1 TUBE | 1 tube | 2024-02-02 | No | No | Historical |
| 72162-1972-3 | 72162197203 | 1 TUBE in 1 CARTON (72162-1972-3) / 30 g in 1 TUBE | 1 tube | 2024-02-02 | No | No | Historical |
| 72162-1972-6 | 72162197206 | 1 TUBE in 1 CARTON (72162-1972-6) / 60 g in 1 TUBE | 1 tube | 2024-02-02 | No | No | Historical |