Details for New Drug Application (NDA): 019451

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NDA 019451 describes LOPRESSIDONE, which is a drug marketed by Novartis and is included in one NDA. Additional details are available on the LOPRESSIDONE profile page.

The generic ingredient in LOPRESSIDONE is chlorthalidone; metoprolol tartrate. There are twenty-one drug master file entries for this compound. Additional details are available on the chlorthalidone; metoprolol tartrate profile page.

Summary for 019451

Tradename:	LOPRESSIDONE
Applicant:	Novartis
Ingredient:	chlorthalidone; metoprolol tartrate
Patents:	0

Profile for product number 001

Active Rx/OTC/Discontinued:	DISCN	Dosage:	CAPSULE;ORAL			Strength	25MG;100MG
Approval Date:	Dec 31, 1987	TE:		RLD:	No

Profile for product number 002

Active Rx/OTC/Discontinued:	DISCN	Dosage:	CAPSULE;ORAL			Strength	25MG;200MG
Approval Date:	Dec 31, 1987	TE:		RLD:	No

Expired US Patents for NDA 019451

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Applicant	Tradename	Generic Name	Dosage	NDA	Approval Date	Patent No.	Patent Expiration
Novartis	LOPRESSIDONE	chlorthalidone; metoprolol tartrate	CAPSULE;ORAL	019451-001	Dec 31, 1987	⤷ Subscribe	⤷ Subscribe
Novartis	LOPRESSIDONE	chlorthalidone; metoprolol tartrate	CAPSULE;ORAL	019451-002	Dec 31, 1987	⤷ Subscribe	⤷ Subscribe
>Applicant	>Tradename	>Generic Name	>Dosage	>NDA	>Approval Date	>Patent No.	>Patent Expiration

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