Last Updated: November 9, 2026

Details for New Drug Application (NDA): 220741

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NDA 220741 describes POMALIDOMIDE, which is a drug marketed by Apotex, Breckenridge, Cipla, Dr Reddys, Eugia Pharma, Hetero Labs Ltd V, MSN, Mylan, Sandoz, Spil, and Teva Pharms Usa, and is included in eleven NDAs. It is available from eleven suppliers. Additional details are available on the POMALIDOMIDE profile page.

The generic ingredient in POMALIDOMIDE is pomalidomide. There is one drug master file entry for this compound. Twelve suppliers are listed for this compound. Additional details are available on the pomalidomide profile page.

Summary for 220741

Tradename:	POMALIDOMIDE
Applicant:	Sandoz
Ingredient:	pomalidomide
Patents:	0

Pharmacology for NDA: 220741

Suppliers and Packaging for NDA: 220741

Tradename	Generic Name	Dosage	NDA	Application Type	Supplier	National Drug Code	Package Code	Package
POMALIDOMIDE	pomalidomide	CAPSULE;ORAL	220741	ANDA	Sandoz Inc	0781-2354	0781-2354-27	21 CAPSULE in 1 BOTTLE (0781-2354-27)
POMALIDOMIDE	pomalidomide	CAPSULE;ORAL	220741	ANDA	Sandoz Inc	0781-2358	0781-2358-27	21 CAPSULE in 1 BOTTLE (0781-2358-27)

Profile for product number 001

Active Rx/OTC/Discontinued:	RX	Dosage:	CAPSULE;ORAL			Strength	1MG
Approval Date:	Aug 31, 2026	TE:	AB	RLD:	No

Profile for product number 002

Active Rx/OTC/Discontinued:	RX	Dosage:	CAPSULE;ORAL			Strength	2MG
Approval Date:	Aug 31, 2026	TE:	AB	RLD:	No

Profile for product number 003

Active Rx/OTC/Discontinued:	RX	Dosage:	CAPSULE;ORAL			Strength	3MG
Approval Date:	Aug 31, 2026	TE:	AB	RLD:	No

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