bortezomib
Generic: bortezomib
Labeler: camber pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
bortezomib
Generic Name
bortezomib
Labeler
camber pharmaceuticals, inc.
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
bortezomib 3.5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
31722-303
Product ID
31722-303_1dd54e11-d200-270e-e063-6394a90a3712
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA212204
Listing Expiration
2026-12-31
Marketing Start
2024-05-03
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
31722303
Hyphenated Format
31722-303
Supplemental Identifiers
RxCUI
UPC
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
ANDA212204 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 3.5 mg/1
Packaging
- 1 VIAL, SINGLE-DOSE in 1 CARTON (31722-303-31) / 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": "1dd54e11-d200-270e-e063-6394a90a3712", "openfda": {"nui": ["N0000175604", "N0000175075"], "upc": ["0331722303316"], "unii": ["69G8BD63PP"], "rxcui": ["402243"], "spl_set_id": ["04aafa6a-a50d-4a47-a831-be8e8bb992ac"], "pharm_class_epc": ["Proteasome Inhibitor [EPC]"], "pharm_class_moa": ["Proteasome Inhibitors [MoA]"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (31722-303-31) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSE", "package_ndc": "31722-303-31", "marketing_start_date": "20240503"}], "brand_name": "Bortezomib", "product_id": "31722-303_1dd54e11-d200-270e-e063-6394a90a3712", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Proteasome Inhibitor [EPC]", "Proteasome Inhibitors [MoA]"], "product_ndc": "31722-303", "generic_name": "Bortezomib", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bortezomib", "active_ingredients": [{"name": "BORTEZOMIB", "strength": "3.5 mg/1"}], "application_number": "ANDA212204", "marketing_category": "ANDA", "marketing_start_date": "20240503", "listing_expiration_date": "20261231"}