Details for New Drug Application (NDA): 019972

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NDA 019972 describes OCUPRESS, which is a drug marketed by Novartis and is included in one NDA. Additional details are available on the OCUPRESS profile page.

The generic ingredient in OCUPRESS is carteolol hydrochloride. There are four drug master file entries for this compound. One supplier is listed for this compound. Additional details are available on the carteolol hydrochloride profile page.

Summary for 019972

Tradename:	OCUPRESS
Applicant:	Novartis
Ingredient:	carteolol hydrochloride
Patents:	0

Medical Subject Heading (MeSH) Categories for 019972

Adrenergic beta-Antagonists
Anti-Arrhythmia Agents
Antihypertensive Agents
Sympatholytics

Profile for product number 001

Active Rx/OTC/Discontinued:	DISCN	Dosage:	SOLUTION/DROPS;OPHTHALMIC			Strength	1% Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons
Approval Date:	May 23, 1990	TE:		RLD:	Yes

Expired US Patents for NDA 019972

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Applicant	Tradename	Generic Name	Dosage	NDA	Approval Date	Patent No.	Patent Expiration
Novartis	OCUPRESS	carteolol hydrochloride	SOLUTION/DROPS;OPHTHALMIC	019972-001	May 23, 1990	3,910,924	⤷ Subscribe
Novartis	OCUPRESS	carteolol hydrochloride	SOLUTION/DROPS;OPHTHALMIC	019972-001	May 23, 1990	4,309,432	⤷ Subscribe
>Applicant	>Tradename	>Generic Name	>Dosage	>NDA	>Approval Date	>Patent No.	>Patent Expiration

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