BETAMETHASONE DIPROPIONATE
- Product NDC
- 71335-2715
- 11-digit product format
- 713352715
- Labeler code
- 71335
- Product ID
- 71335-2715_c83c993e-71a3-41b4-8d09-0dd5cfbcae22
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- betamethasone dipropionate
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA215847
- Marketing category
- ANDA
- Marketing start
- 2022-05-20
- Substance
- BETAMETHASONE DIPROPIONATE
- Active strength
- .5 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
openFDA Listing Details
- Product ID
- 71335-2715_c83c993e-71a3-41b4-8d09-0dd5cfbcae22
- Product type
- HUMAN PRESCRIPTION DRUG
- Finished product
- Yes
- Brand name base
- BETAMETHASONE DIPROPIONATE
- Generic name
- betamethasone dipropionate
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Marketing start
- 2022-05-20
- Marketing category
- ANDA
- Application number
- ANDA215847
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA]; Corticosteroid [EPC]
- Listing expiration
- 2026-12-31
openFDA Active Ingredients
| Ingredient | Strength |
|---|
| BETAMETHASONE DIPROPIONATE | .5 mg/g |
openFDA Harmonized Identifiers
| Field | Values |
|---|
| Unii | 826Y60901U |
| Rxcui | 197405 |
| Spl Set Id | 52c0e92f-986e-45e7-99cf-9a13ac386b1d |
| Manufacturer Name | Bryant Ranch Prepack |
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 826Y60901U | BETAMETHASONE DIPROPIONATE | 5593-20-4 | BETAMETHASONE DIPROPIONATE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2715-1 | 71335271501 | 1 TUBE in 1 CARTON (71335-2715-1) / 45 g in 1 TUBE | 1 tube | 2025-07-28 | No | No | Current |