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Last Updated: November 22, 2024

Details for New Drug Application (NDA): 074851

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NDA 074851 describes LEVOBUNOLOL HYDROCHLORIDE, which is a drug marketed by Alcon Labs Inc, Apotex Inc, Bausch And Lomb, and Chartwell Rx, and is included in six NDAs. It is available from one supplier. Additional details are available on the LEVOBUNOLOL HYDROCHLORIDE profile page.

The generic ingredient in LEVOBUNOLOL HYDROCHLORIDE is levobunolol hydrochloride. There are seven drug master file entries for this compound. One supplier is listed for this compound. Additional details are available on the levobunolol hydrochloride profile page.

Summary for 074851

Tradename:	LEVOBUNOLOL HYDROCHLORIDE
Applicant:	Alcon Labs Inc
Ingredient:	levobunolol hydrochloride
Patents:	0

Medical Subject Heading (MeSH) Categories for 074851

Adrenergic beta-Antagonists
Sympatholytics

Profile for product number 001

Active Rx/OTC/Discontinued:	DISCN	Dosage:	SOLUTION/DROPS;OPHTHALMIC			Strength	0.25%
Approval Date:	Oct 28, 1996	TE:		RLD:	No

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