Betamethasone Dipropionate
- Product NDC
- 50090-5260
- 11-digit product format
- 500905260
- Labeler code
- 50090
- Product ID
- 50090-5260_59afe479-36aa-493b-ad85-1dd0df9e9359
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Betamethasone Dipropionate
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA210217
- Marketing category
- ANDA
- Marketing start
- 2018-10-12
- Marketing end
- 0000-00-00
- Substance
- BETAMETHASONE DIPROPIONATE
- Active strength
- 1 mg/g
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
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 | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-5260-0 | 50090526000 | 1 TUBE in 1 CARTON (50090-5260-0) > 15 g in 1 TUBE | 1 tube | 2020-10-15 | 0000-00-00 | No | No | Current |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Betamethasone Dipropionate | A-S Medication Solutions | 2021-01-15 | HUMAN PRESCRIPTION DRUG LABEL | 1 |