bortezomib
Generic: bortezomib
Labeler: hospira, inc.Drug Facts
Product Profile
Brand Name
bortezomib
Generic Name
bortezomib
Labeler
hospira, inc.
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
bortezomib 1 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0409-1704
Product ID
0409-1704_e7c31651-e301-43f9-bc81-e0fd5dcb828c
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA209191
Listing Expiration
2026-12-31
Marketing Start
2022-05-16
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
04091704
Hyphenated Format
0409-1704
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
bortezomib (source: ndc)
Generic Name
bortezomib (source: ndc)
Application Number
NDA209191 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/1
Packaging
- 1 VIAL, SINGLE-DOSE in 1 CARTON (0409-1704-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "e7c31651-e301-43f9-bc81-e0fd5dcb828c", "openfda": {"nui": ["N0000175604", "N0000175075"], "unii": ["69G8BD63PP"], "rxcui": ["2601542", "2601544"], "spl_set_id": ["9fdf6169-699f-40eb-bda1-760253062b3c"], "pharm_class_epc": ["Proteasome Inhibitor [EPC]"], "pharm_class_moa": ["Proteasome Inhibitors [MoA]"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (0409-1704-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSE", "package_ndc": "0409-1704-01", "marketing_start_date": "20220516"}], "brand_name": "BORTEZOMIB", "product_id": "0409-1704_e7c31651-e301-43f9-bc81-e0fd5dcb828c", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Proteasome Inhibitor [EPC]", "Proteasome Inhibitors [MoA]"], "product_ndc": "0409-1704", "generic_name": "BORTEZOMIB", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BORTEZOMIB", "active_ingredients": [{"name": "BORTEZOMIB", "strength": "1 mg/1"}], "application_number": "NDA209191", "marketing_category": "NDA", "marketing_start_date": "20220516", "listing_expiration_date": "20261231"}