bortezomib
Generic: bortezomib
Labeler: sintetica us llcDrug Facts
Product Profile
Brand Name
bortezomib
Generic Name
bortezomib
Labeler
sintetica us llc
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
bortezomib 3.5 mg/3.5mL
Manufacturer
Identifiers & Regulatory
Product NDC
83090-008
Product ID
83090-008_074a288f-8a8f-7c41-e063-6294a90a68dc
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA209622
Listing Expiration
2026-12-31
Marketing Start
2023-07-15
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
83090008
Hyphenated Format
83090-008
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
ANDA209622 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 3.5 mg/3.5mL
Packaging
- 1 VIAL, SINGLE-DOSE in 1 CARTON (83090-008-01) / 3.5 mL 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": "074a288f-8a8f-7c41-e063-6294a90a68dc", "openfda": {"nui": ["N0000175604", "N0000175075"], "unii": ["69G8BD63PP"], "rxcui": ["402243"], "spl_set_id": ["d79a71ec-b46d-4961-ad05-8980915cba94"], "pharm_class_epc": ["Proteasome Inhibitor [EPC]"], "pharm_class_moa": ["Proteasome Inhibitors [MoA]"], "manufacturer_name": ["Sintetica US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (83090-008-01) / 3.5 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "83090-008-01", "marketing_start_date": "20230715"}], "brand_name": "Bortezomib", "product_id": "83090-008_074a288f-8a8f-7c41-e063-6294a90a68dc", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Proteasome Inhibitor [EPC]", "Proteasome Inhibitors [MoA]"], "product_ndc": "83090-008", "generic_name": "Bortezomib", "labeler_name": "Sintetica US LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bortezomib", "active_ingredients": [{"name": "BORTEZOMIB", "strength": "3.5 mg/3.5mL"}], "application_number": "ANDA209622", "marketing_category": "ANDA", "marketing_start_date": "20230715", "listing_expiration_date": "20261231"}