Betamethasone Valerate
- Product NDC
- 50742-315
- 11-digit product format
- 507420315
- Labeler code
- 50742
- Product ID
- 50742-315_d4322137-1b63-4534-aa14-920c7b1b4313
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Betamethasone Valerate
- Dosage form
- AEROSOL, FOAM
- Route
- TOPICAL
- Labeler
- Ingenus Pharmaceuticals, LLC
- Application
- ANDA207144
- Marketing category
- ANDA
- Marketing start
- 2017-05-25
- Marketing end
- 2023-04-30
- Substance
- BETAMETHASONE VALERATE
- Active strength
- 1 mg/g
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50742-315-01 | 50742031501 | 1 CAN in 1 CARTON (50742-315-01) > 100 g in 1 CAN | 1 can | 2017-05-25 | 2023-04-30 | No | No | Current |
| 50742-315-50 | 50742031550 | 1 CAN in 1 CARTON (50742-315-50) > 50 g in 1 CAN | 1 can | 2017-05-25 | 2023-04-30 | No | No | Current |