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Last Updated: November 22, 2024

Details for New Drug Application (NDA): 204740

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NDA 204740 describes IRBESARTAN, which is a drug marketed by Ajanta Pharma Ltd, Alembic Pharms Ltd, Amneal Pharms, Apotex Inc, Aurobindo Pharma Ltd, Chartwell Molecular, Chartwell Rx, Hetero Labs Ltd V, Hikma, Hisun Pharm Hangzhou, Ipca Labs Ltd, Jubilant Generics, Lupin Ltd, Macleods Pharms Ltd, Prinston Inc, Sandoz, Sciegen Pharms Inc, Teva Pharms, Unichem, Upsher Smith Labs, Watson Labs Inc, Zydus Pharms Usa Inc, Alembic, Atlas Pharms Llc, Dr Reddys Labs Ltd, Norvium Bioscience, and Teva, and is included in thirty-seven NDAs. It is available from twenty-one suppliers. Additional details are available on the IRBESARTAN profile page.

The generic ingredient in IRBESARTAN is hydrochlorothiazide; irbesartan. There are thirty-two drug master file entries for this compound. Thirteen suppliers are listed for this compound. Additional details are available on the hydrochlorothiazide; irbesartan profile page.

Summary for 204740

Tradename:	IRBESARTAN
Applicant:	Amneal Pharms
Ingredient:	irbesartan
Patents:	0

Pharmacology for NDA: 204740

Mechanism of Action	Angiotensin 2 Receptor Antagonists

Suppliers and Packaging for NDA: 204740

Tradename	Generic Name	Dosage	NDA	Application Type	Supplier	National Drug Code	Package Code	Package
IRBESARTAN	irbesartan	TABLET;ORAL	204740	ANDA	Amneal Pharmaceuticals LLC	65162-284	65162-284-03	30 TABLET in 1 BOTTLE (65162-284-03)
IRBESARTAN	irbesartan	TABLET;ORAL	204740	ANDA	Amneal Pharmaceuticals LLC	65162-284	65162-284-09	90 TABLET in 1 BOTTLE (65162-284-09)

Profile for product number 001

Active Rx/OTC/Discontinued:	RX	Dosage:	TABLET;ORAL			Strength	75MG
Approval Date:	Apr 17, 2018	TE:	AB	RLD:	No

Profile for product number 002

Active Rx/OTC/Discontinued:	RX	Dosage:	TABLET;ORAL			Strength	150MG
Approval Date:	Apr 17, 2018	TE:	AB	RLD:	No

Profile for product number 003

Active Rx/OTC/Discontinued:	RX	Dosage:	TABLET;ORAL			Strength	300MG
Approval Date:	Apr 17, 2018	TE:	AB	RLD:	No

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