BORTEZOMIB

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: BORTEZOMIB
Generic name: BORTEZOMIB
Manufacturer: Zydus Lifesciences Limited
Product type: HUMAN PRESCRIPTION DRUG
SPL set ID: 582c7c0d-fa25-4586-8157-a1e2653d72d9
SPL ID: a7ff2205-566b-4fb5-8f33-bf73377ee093
Version: 1
Effective date: 2022-05-05
Source export date: 2026-10-12
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:39:59

Harmonized routes table
Harmonized routes
INTRAVENOUS, SUBCUTANEOUS

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 12 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application applno	ANDA	210204	derived:openfda.application_number
application number		ANDA210204	openfda.application_number
brand name		BORTEZOMIB	openfda.brand_name
generic name		BORTEZOMIB	openfda.generic_name
manufacturer name		Zydus Lifesciences Limited	openfda.manufacturer_name
ndc	package	70771-1708-1	openfda.package_ndc
ndc	product	70771-1708	openfda.product_ndc
ndc11	package	70771170801	derived:openfda.package_ndc
rxcui		402243	openfda.rxcui
spl id		a7ff2205-566b-4fb5-8f33-bf73377ee093	id
spl set id		582c7c0d-fa25-4586-8157-a1e2653d72d9	set_id
unii		69G8BD63PP	openfda.unii

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