Details for New Drug Application (NDA): 212773

NDA 212773 describes IMATINIB MESYLATE, which is a drug marketed by Amneal Pharms, Apotex, Breckenridge, Chartwell Rx, Dr Reddys, Eugia Pharma, Hikma, Mylan, Natco Pharma Ltd, Qilu Pharm Hainan, Shilpa, Sun Pharm, Teva Pharms Usa, and Zydus Pharms, and is included in fourteen NDAs. It is available from twenty-two suppliers. Additional details are available on the IMATINIB MESYLATE profile page.

The generic ingredient in IMATINIB MESYLATE is imatinib mesylate. There are thirty-four drug master file entries for this compound. Twenty-three suppliers are listed for this compound. Additional details are available on the imatinib mesylate profile page.

Summary for 212773

Tradename:	IMATINIB MESYLATE
Applicant:	Eugia Pharma
Ingredient:	imatinib mesylate
Patents:	0

Pharmacology for NDA: 212773

Mechanism of Action

Bcr-Abl Tyrosine Kinase Inhibitors Cytochrome P450 2D6 Inhibitors Cytochrome P450 3A4 Inhibitors

Medical Subject Heading (MeSH) Categories for 212773

Antineoplastic Agents

Protein Kinase Inhibitors

Suppliers and Packaging for NDA: 212773

Tradename	Generic Name	Dosage	NDA	Application Type	Supplier	National Drug Code	Package Code	Package
IMATINIB MESYLATE	imatinib mesylate	TABLET;ORAL	212773	ANDA	Aurobindo Pharma Limited	59651-240	59651-240-90	90 TABLET, FILM COATED in 1 BOTTLE (59651-240-90)
IMATINIB MESYLATE	imatinib mesylate	TABLET;ORAL	212773	ANDA	Aurobindo Pharma Limited	59651-241	59651-241-03	3 BLISTER PACK in 1 CARTON (59651-241-03) / 10 TABLET, FILM COATED in 1 BLISTER PACK

Profile for product number 001

Active Rx/OTC/Discontinued:	RX	Dosage:	TABLET;ORAL			Strength	EQ 100MG BASE
Approval Date:	Jul 23, 2020	TE:	AB	RLD:	No

Profile for product number 002

Active Rx/OTC/Discontinued:	RX	Dosage:	TABLET;ORAL			Strength	EQ 400MG BASE
Approval Date:	Jul 23, 2020	TE:	AB	RLD:	No

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