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Last Updated: December 16, 2025

Details for New Drug Application (NDA): 207022

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NDA 207022 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. Eight suppliers are listed for this compound. Additional details are available on the mycophenolate mofetil hydrochloride profile page.

Summary for 207022

Tradename:	MYCOPHENOLATE MOFETIL
Applicant:	Hetero Labs Ltd V
Ingredient:	mycophenolate mofetil
Patents:	0

Pharmacology for NDA: 207022

Suppliers and Packaging for NDA: 207022

Tradename	Generic Name	Dosage	NDA	Application Type	Supplier	National Drug Code	Package Code	Package
MYCOPHENOLATE MOFETIL	mycophenolate mofetil	CAPSULE;ORAL	207022	ANDA	Camber Pharmaceuticals, Inc.	31722-878	31722-878-01	1 BOTTLE in 1 CARTON (31722-878-01) / 100 CAPSULE in 1 BOTTLE
MYCOPHENOLATE MOFETIL	mycophenolate mofetil	CAPSULE;ORAL	207022	ANDA	Camber Pharmaceuticals, Inc.	31722-878	31722-878-05	500 CAPSULE in 1 BOTTLE (31722-878-05)

Profile for product number 001

Active Rx/OTC/Discontinued:	RX	Dosage:	CAPSULE;ORAL			Strength	250MG
Approval Date:	Oct 22, 2024	TE:	AB	RLD:	No

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