bortezomib
Generic: bortezomib
Labeler: bluepoint laboratoriesDrug Facts
Product Profile
Brand Name
bortezomib
Generic Name
bortezomib
Labeler
bluepoint laboratories
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
bortezomib 3.5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68001-540
Product ID
68001-540_df1f04a5-b5bc-73e6-e053-2a95a90aa6d4
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210824
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
68001540
Hyphenated Format
68001-540
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
ANDA210824 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 3.5 mg/1
Packaging
- 1 VIAL in 1 CARTON (68001-540-36) / 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": "df1f04a5-b5bc-73e6-e053-2a95a90aa6d4", "openfda": {"nui": ["N0000175604", "N0000175075"], "unii": ["69G8BD63PP"], "rxcui": ["402243"], "spl_set_id": ["12500f21-8e2f-4bcd-861e-4dfca843da2e"], "pharm_class_epc": ["Proteasome Inhibitor [EPC]"], "pharm_class_moa": ["Proteasome Inhibitors [MoA]"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (68001-540-36) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL", "package_ndc": "68001-540-36", "marketing_start_date": "20220516"}], "brand_name": "Bortezomib", "product_id": "68001-540_df1f04a5-b5bc-73e6-e053-2a95a90aa6d4", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Proteasome Inhibitor [EPC]", "Proteasome Inhibitors [MoA]"], "product_ndc": "68001-540", "generic_name": "Bortezomib", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bortezomib", "active_ingredients": [{"name": "BORTEZOMIB", "strength": "3.5 mg/1"}], "application_number": "ANDA210824", "marketing_category": "ANDA", "marketing_start_date": "20220516", "listing_expiration_date": "20261231"}