NDC 86032-031-01 - Chlorambucil

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 86032-031
Requested NDC: 86032-031-01
Package NDCs from labels: 86032-031-01
Manufacturer: Evereen Shanghai Biotechnology Ltd. | Newstarpharm Technology Limited
Effective date: 2024-11-25
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Chlorambucil	Evereen Shanghai Biotechnology Ltd. \| Newstarpharm Technology Limited	2024-11-25	BULK INGREDIENT - ANIMAL DRUG

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
86032-031-01	Chlorambucil	100 g in 1 BAG	POWDER	100		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
86032-031	CHLORAMBUCIL POWDER [EVEREEN SHANGHAI BIOTECHNOLOGY LTD.]	1	1 package rows	20241127_9d7810fc-c452-46c6-8987-731e2f2b3e9e.zip

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 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
LEUKERAN	CHLORAMBUCIL	Waylis Therapeutics LLC	58a3c995-5ad6-465d-8437-5970c9088213	2025-01-08	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: 18D0SL7309

Reported adverse events (FAERS/openFDA)#

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