LUMOXITI
- Product NDC
- 0310-4700
- 11-digit product format
- 003104700
- Labeler code
- 0310
- Product ID
- 0310-4700_a9e94288-ebc3-49b7-b07b-9f2cd4439631
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- moxetumomab pasudotox
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- AstraZeneca Pharmaceuticals LP
- Application
- BLA761104
- Marketing category
- BLA
- Marketing start
- 2018-10-24
- Marketing end
- 0000-00-00
- Substance
- MOXETUMOMAB PASUDOTOX
- Active strength
- 1 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 0310-4700-01 | 00310470001 | 1 VIAL in 1 CARTON (0310-4700-01) > 1 mL in 1 VIAL | 1 vial | 2018-10-24 | 0000-00-00 | No | No | Current |