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Last Updated: March 19, 2026

Details for New Drug Application (NDA): 217828

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NDA 217828 describes MYCOPHENOLATE MOFETIL, which is a drug marketed by Accord Hlthcare, Alkem Labs Ltd, Apotex Corp, Aurobindo Pharma Ltd, Concord Biotech Ltd, Dr Reddys Labs Ltd, Hetero Labs Ltd V, Hikma, Jubilant Cadista, Mylan, Sandoz, Strides Pharma, Strides Pharma Intl, Teva Pharms, Wuxi, Zhejiang Hisun Pharm, Zydus Pharms Usa Inc, Amneal, Lannett Co Inc, Rising, Teva Pharms Usa, Vistapharm Llc, Apotex, Aurobindo Pharma, Bpi Labs, Meitheal, Mylan Labs Ltd, Onesource Specialty, Ph Health, and Zydus Pharms, and is included in forty-nine NDAs. It is available from twenty-nine suppliers. Additional details are available on the MYCOPHENOLATE MOFETIL profile page.

The generic ingredient in MYCOPHENOLATE MOFETIL is mycophenolate mofetil hydrochloride. There are thirty-eight drug master file entries for this compound. Seven suppliers are listed for this compound. Additional details are available on the mycophenolate mofetil hydrochloride profile page.

Summary for 217828

Tradename:	MYCOPHENOLATE MOFETIL
Applicant:	Aurobindo Pharma Ltd
Ingredient:	mycophenolate mofetil
Patents:	0

Pharmacology for NDA: 217828

Suppliers and Packaging for NDA: 217828

Tradename	Generic Name	Dosage	NDA	Application Type	Supplier	National Drug Code	Package Code	Package
MYCOPHENOLATE MOFETIL	mycophenolate mofetil	CAPSULE;ORAL	217828	ANDA	Aurobindo Pharma Limited	59651-624	59651-624-01	100 CAPSULE in 1 BOTTLE (59651-624-01)
MYCOPHENOLATE MOFETIL	mycophenolate mofetil	CAPSULE;ORAL	217828	ANDA	Aurobindo Pharma Limited	59651-624	59651-624-05	500 CAPSULE in 1 BOTTLE (59651-624-05)

Profile for product number 001

Active Rx/OTC/Discontinued:	RX	Dosage:	CAPSULE;ORAL			Strength	250MG
Approval Date:	Jan 5, 2024	TE:	AB	RLD:	No

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