Lomustine

Manufacturer
H3 Medical Inc
Effective date
2018-07-13
Label type
BULK INGREDIENT
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:53:27

Label at a glance#

ProductLomustine
Active ingredientLOMUSTINE
Label structure1 sections

Label contents#

Full prescribing information#

Product Label-Lomustine

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 1 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63732-204463732-2044-3, 63732-2044-4, 63732-2044-5, 63732-2044-6

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 1 matching rows.

Name, UNII, Kind table
NameUNIIKind
LOMUSTINE7BRF0Z81KGACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 4 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
LomustineLOMUSTINEWilshire Pharmaceuticals, Inc.3c3637fc-4499-4331-a3c4-6969fc86704e2026-02-12Boxed warning, Warnings, Adverse reactionsName fallback
brand name: Lomustine
generic name: LOMUSTINE
LOMUSTINELOMUSTINECarnegie Pharmaceuticals LLC916dfac8-da11-40e4-9e44-a909e29a6b5f2025-10-28Boxed warning, Warnings, Adverse reactionsName fallback
brand name: LOMUSTINE
generic name: LOMUSTINE
GleostineLOMUSTINEAzurity Pharmaceuticals, Inc.3529fe2f-3c23-4862-bb20-b480269570822025-09-25Boxed warning, Warnings, Adverse reactionsName fallback
generic name: LOMUSTINE
GleostineLOMUSTINENextSource Biotechnology, LLC7f77526b-4c40-409c-82ea-d0f934d89cc22024-01-23Boxed warning, Warnings, Adverse reactionsName fallback
generic name: LOMUSTINE

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.