bortezomib
Generic: bortezomib
Labeler: waverley pharma incDrug Facts
Product Profile
Brand Name
bortezomib
Generic Name
bortezomib
Labeler
waverley pharma inc
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
bortezomib 3.5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72338-200
Product ID
72338-200_c7ce3b3b-d310-47b5-9173-e84abab715f6
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA211898
Listing Expiration
2026-12-31
Marketing Start
2018-06-19
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72338200
Hyphenated Format
72338-200
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
ANDA211898 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 3.5 mg/1
Packaging
- 1 VIAL in 1 CARTON (72338-200-01) / 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": "c7ce3b3b-d310-47b5-9173-e84abab715f6", "openfda": {"nui": ["N0000175604", "N0000175075"], "upc": ["0372338200019"], "unii": ["69G8BD63PP"], "rxcui": ["402243"], "spl_set_id": ["a73d7ea7-d068-4d25-b368-fc3db1898be2"], "pharm_class_epc": ["Proteasome Inhibitor [EPC]"], "pharm_class_moa": ["Proteasome Inhibitors [MoA]"], "manufacturer_name": ["Waverley Pharma Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (72338-200-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL", "package_ndc": "72338-200-01", "marketing_start_date": "20180619"}], "brand_name": "Bortezomib", "product_id": "72338-200_c7ce3b3b-d310-47b5-9173-e84abab715f6", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Proteasome Inhibitor [EPC]", "Proteasome Inhibitors [MoA]"], "product_ndc": "72338-200", "generic_name": "bortezomib", "labeler_name": "Waverley Pharma Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bortezomib", "active_ingredients": [{"name": "BORTEZOMIB", "strength": "3.5 mg/1"}], "application_number": "ANDA211898", "marketing_category": "ANDA", "marketing_start_date": "20180619", "listing_expiration_date": "20261231"}