Betamethasone Dipropionate
- Product NDC
- 72162-1405
- 11-digit product format
- 721621405
- Labeler code
- 72162
- Product ID
- 72162-1405_e217657e-f77b-4060-bc6c-ef208fbccdba
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Betamethasone Dipropionate
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076592
- Marketing category
- ANDA
- Marketing start
- 2006-09-28
- 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
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 |
|---|
| 72162-1405-2 | 72162140502 | 1 TUBE in 1 CARTON (72162-1405-2) / 15 g in 1 TUBE | 1 tube | 2024-03-11 | No | No | Historical |
| 72162-1405-4 | 72162140504 | 1 TUBE in 1 CARTON (72162-1405-4) / 50 g in 1 TUBE | 1 tube | 2024-03-11 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Betamethasone Dipropionate | Bryant Ranch Prepack | 2025-08-07 | HUMAN PRESCRIPTION DRUG LABEL | 102 |