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Last Updated: December 12, 2025

Details for New Drug Application (NDA): 218142

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NDA 218142 describes ERIBULIN MESYLATE, which is a drug marketed by Baxter Hlthcare Corp, Chia Tai Tianqing, Dr Reddys, Gland, Glenmark Pharms Inc, Jiangxi Kvvit Pharm, Long Grove Pharms, and Sandoz, and is included in eight NDAs. It is available from twelve suppliers. Additional details are available on the ERIBULIN MESYLATE profile page.

The generic ingredient in ERIBULIN MESYLATE is eribulin mesylate. Fourteen suppliers are listed for this compound. Additional details are available on the eribulin mesylate profile page.

Summary for 218142

Tradename:	ERIBULIN MESYLATE
Applicant:	Glenmark Pharms Inc
Ingredient:	eribulin mesylate
Patents:	0

Pharmacology for NDA: 218142

Physiological Effect	Microtubule Inhibition

Suppliers and Packaging for NDA: 218142

Tradename	Generic Name	Dosage	NDA	Application Type	Supplier	National Drug Code	Package Code	Package
ERIBULIN MESYLATE	eribulin mesylate	SOLUTION;INTRAVENOUS	218142	ANDA	Kindos Pharmaceuticals Co., Ltd.	40033-364	40033-364-01	1 VIAL, SINGLE-DOSE in 1 CARTON (40033-364-01) / 2 mL in 1 VIAL, SINGLE-DOSE
ERIBULIN MESYLATE	eribulin mesylate	SOLUTION;INTRAVENOUS	218142	ANDA	GLENMARK PHARMACEUTICALS INC., USA	68462-770	68462-770-20	1 VIAL, SINGLE-DOSE in 1 CARTON (68462-770-20) / 2 mL in 1 VIAL, SINGLE-DOSE

Profile for product number 001

Active Rx/OTC/Discontinued:	RX	Dosage:	SOLUTION;INTRAVENOUS			Strength	1MG/2ML (0.5MG/ML)
Approval Date:	Aug 5, 2025	TE:	AP	RLD:	No

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