NDC 73377-215-01 - sorafenib Tosylate

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: 73377-215
Requested NDC: 73377-215-01
Package NDCs from labels: 73377-215-01, 73377-215-02, 73377-215-03
Manufacturer: AX Pharmaceutical Corp
Effective date: 2023-08-29
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
sorafenib Tosylate - AX Pharmaceutical Corp	AX Pharmaceutical Corp	2023-08-29	BULK INGREDIENT - ANIMAL DRUG

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
73377-215-01	sorafenib Tosylate	1000 g in 1 JAR	POWDER	1000	2
73377-215-02	sorafenib Tosylate	500 g in 1 JAR	POWDER	500	2
73377-215-03	sorafenib Tosylate	350 g in 1 JAR	POWDER	350	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73377-215	SORAFENIB TOSYLATE POWDER [AX PHARMACEUTICAL CORP]	2	3 package rows	20230830_207725a4-e108-4afd-8c98-9abbe087126e.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 · 3 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Sorafenib Tosylate	SORAFENIB	Mylan Pharmaceuticals Inc.	b7919013-1511-44f0-a759-3fa78a9fa178	2026-03-18	Warnings, Adverse reactions	Exact identifier unii: 5T62Q3B36J
sorafenib	SORAFENIB	Dr.Reddys Laboratories Inc	93f9c3b2-d4c5-80d3-5421-8b4c29fbf8a6	2024-12-02	Warnings, Adverse reactions	Exact identifier unii: 5T62Q3B36J
Sorafenib	SORAFENIB	Teva Pharmaceuticals, Inc.	dae598f7-823f-405c-ae31-f924594187b9	2022-07-01	Warnings, Adverse reactions	Exact identifier unii: 5T62Q3B36J

Reported adverse events (FAERS/openFDA)#

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