betamethasone dipropionate
- Product NDC
- 70771-1550
- 11-digit product format
- 707711550
- Labeler code
- 70771
- Product ID
- 70771-1550_34685b34-d41c-4a8b-b6db-9cd17e4ced70
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- betamethasone dipropionate
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Zydus Lifesciences Limited
- Application
- ANDA214048
- Marketing category
- ANDA
- Marketing start
- 2020-07-20
- 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 |
|---|
| 70771-1550-1 | 70771155001 | 1 TUBE in 1 CARTON (70771-1550-1) / 15 g in 1 TUBE | 1 tube | 2020-07-20 | No | No | Historical |
| 70771-1550-4 | 70771155004 | 1 TUBE in 1 CARTON (70771-1550-4) / 45 g in 1 TUBE | 1 tube | 2020-07-20 | No | No | Historical |