BETAMETHASONE DIPROPIONATE
- Product NDC
- 63629-9324
- 11-digit product format
- 636299324
- Labeler code
- 63629
- Product ID
- 63629-9324_16dc1c3b-a6dd-474d-b765-01d7862bc5de
- 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
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 |
|---|
| 63629-9324-1 | 63629932401 | 1 TUBE in 1 CARTON (63629-9324-1) / 45 g in 1 TUBE | 1 tube | 2022-07-07 | No | No | Historical |