Bortezomib 3.5 mg / 1 Injection 1 Vial, Single-Dose
Reference details for licensed healthcare facility review and verification.
| NDC 11 | 00409-1700-01 |
|---|---|
| Product NDC | 00409-1700 |
| Generic Drug Name | Bortezomib |
| Brand Name | Bortezomib |
| Manufacturer | Hospira, Inc. |
| Strength | 3.5 mg / 1 |
| Dosage Form | Injection |
| Drug Type | Intravenous; Subcutaneous |
| Package Quantity | 1 Vial, Single-Dose |
| Package Description | 1 VIAL, SINGLE-DOSE in 1 CARTON (0409-1700-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSE |
| Active Ingredients | Bortezomib |
| Marketing Category | ANDA |
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NDC snapshot
Bortezomib 3.5 mg / 1 Injection is tracked under NDC 00409-1700-01 and rolls up into product family 00409-1700. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.
- Package configuration: 1 Vial, Single-Dose.
- Manufacturer: Hospira, Inc..
- Dosage form: Injection.
- Family size: 1 indexed presentation.
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Official references
Use official labeling and directory references to confirm presentation details while your team reviews the PRN catalog entry and related sourcing paths.
Potential alternatives with matching presentation
Open the comparison hub or review package-level listings from 6 product-NDC families with matching normalized presentation details. Review each product detail page before treating any item as a true alternative.
Bortezomib 3.5 mg / 1 Injection 1 Vial, Single-Dose, NDC 00409-1700-01, is a Hospira, Inc. 3.5 mg / 1 injection presentation packaged as 1 Vial, Single-Dose.
NDC search formats
- Canonical NDC 11: 00409-1700-01
- Digits-only NDC 11: 00409170001
- Possible 10-digit display formats: 0409-1700-01 (0409170001), 00409-1700-1 (0040917001)
Multiple 10-digit display-format aliases can map to the same stored 11-digit billing NDC, so these are shown as search aliases rather than a single asserted package format.
Helpful product links
- Search by brand name: Bortezomib
- NDC 11: 00409-1700-01
- Product family NDC: 00409-1700
- VA classification code: AN900
- VA classification code description: ANTINEOPLASTIC,OTHER
- CMOP ID: B0873
- VUID: 4037651