Blenrep
- Product NDC
- 0173-0896
- 11-digit product format
- 001730896
- Labeler code
- 0173
- Product ID
- 0173-0896_15fcefaf-72a9-438a-aaa5-39e2227375b1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Belantamab
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- GlaxoSmithKline LLC
- Application
- BLA761158
- Marketing category
- BLA
- Marketing start
- 2020-08-05
- Marketing end
- 0000-00-00
- Substance
- BELANTAMAB MAFODOTIN
- Active strength
- 50 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 |
|---|
| 0173-0896-01 | 00173089601 | 1 VIAL in 1 CARTON (0173-0896-01) > 2 mL in 1 VIAL | 1 vial | 2020-08-05 | 0000-00-00 | No | No | Current |