bortezomib
Generic: bortezomib
Labeler: pharmascience inc.Drug Facts
Product Profile
Brand Name
bortezomib
Generic Name
bortezomib
Labeler
pharmascience inc.
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
bortezomib 3.5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
51817-586
Product ID
51817-586_de0c8157-9e0e-4964-e053-2995a90a1259
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA208392
Listing Expiration
2026-12-31
Marketing Start
2022-05-02
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
51817586
Hyphenated Format
51817-586
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
ANDA208392 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 3.5 mg/1
Packaging
- 1 VIAL in 1 CARTON (51817-586-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "de0c8157-9e0e-4964-e053-2995a90a1259", "openfda": {"nui": ["N0000175604", "N0000175075"], "unii": ["69G8BD63PP"], "rxcui": ["402243"], "spl_set_id": ["191d231a-1fbd-4a65-9d33-d5dc03bac381"], "pharm_class_epc": ["Proteasome Inhibitor [EPC]"], "pharm_class_moa": ["Proteasome Inhibitors [MoA]"], "manufacturer_name": ["Pharmascience Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (51817-586-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL", "package_ndc": "51817-586-01", "marketing_start_date": "20220502"}], "brand_name": "Bortezomib", "product_id": "51817-586_de0c8157-9e0e-4964-e053-2995a90a1259", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Proteasome Inhibitor [EPC]", "Proteasome Inhibitors [MoA]"], "product_ndc": "51817-586", "generic_name": "bortezomib", "labeler_name": "Pharmascience Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bortezomib", "active_ingredients": [{"name": "BORTEZOMIB", "strength": "3.5 mg/1"}], "application_number": "ANDA208392", "marketing_category": "ANDA", "marketing_start_date": "20220502", "listing_expiration_date": "20261231"}