Betamethasone Valerate
- Product NDC
- 70518-3137
- 11-digit product format
- 705183137
- Labeler code
- 70518
- Product ID
- 70518-3137_e38812d0-fa86-5b94-e053-2995a90aa240
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Betamethasone Valerate
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- REMEDYREPACK INC.
- Application
- NDA018642
- Marketing category
- NDA
- Marketing start
- 2021-06-30
- Marketing end
- 0000-00-00
- Substance
- BETAMETHASONE VALERATE
- Active strength
- 1 mg/g
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 9IFA5XM7R2 | BETAMETHASONE VALERATE | 2152-44-5 | BETAMETHASONE VALERATE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3137-0 | 70518313700 | 1 TUBE in 1 CARTON (70518-3137-0) > 15 g in 1 TUBE | 1 tube | 2021-06-30 | 0000-00-00 | No | No | Current |