bortezomib

Generic: bortezomib

Labeler: waverley pharma inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name bortezomib
Generic Name bortezomib
Labeler waverley pharma inc
Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
INTRAVENOUS SUBCUTANEOUS
Active Ingredients

bortezomib 3.5 mg/1

Manufacturer
Waverley Pharma Inc

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)
proteasome inhibitor [epc]
Mechanism of Action
proteasome inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72338200
Hyphenated Format 72338-200

Supplemental Identifiers

RxCUI
402243
UPC
0372338200019
UNII
69G8BD63PP
NUI
N0000175604 N0000175075

Packaging Origin

Original Packager
true

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
INTRAVENOUS SUBCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • 3.5 mg/1
source: ndc
Packaging
  • 1 VIAL in 1 CARTON (72338-200-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL
source: ndc

Packages (1)

Ingredients (1)

bortezomib (3.5 mg/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"}