LUMOXITI
- Product NDC
- 73380-4700
- 11-digit product format
- 733804700
- Labeler code
- 73380
- Product ID
- 73380-4700_50a54d82-8f62-4e80-a35f-cd51a48bb0e5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- MOXETUMOMAB PASUDOTOX
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Innate Pharma, Inc.
- Application
- BLA761104
- Marketing category
- BLA
- Marketing start
- 2020-05-15
- Marketing end
- 0000-00-00
- Substance
- MOXETUMOMAB PASUDOTOX
- Active strength
- 1 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 73380-4700-1 | LUMOXITI | 1 mL in 1 VIAL | INJECTION, POWDER, LYOPHILIZED, | 1 | | 2 |
| 73380-4700-1 | LUMOXITI | 1 in 1 CARTON | INJECTION, POWDER, LYOPHILIZED, | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 73380-4700 | LUMOXITI (MOXETUMOMAB PASUDOTOX) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION IV STABILIZER (POLYSORBATE 80) SOLUTION [INNATE PHARMA, INC.] | 2 | Legacy NDC, 2 package rows | 20200905_8ddffb08-aab1-41f5-bbc6-09457e4e80ca.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 73380-4700-1 | 73380470001 | 1 VIAL in 1 CARTON (73380-4700-1) > 1 mL in 1 VIAL | 1 vial | 2020-05-15 | 0000-00-00 | No | No | Current |