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LEVOBUNOLOL HYDROCHLORIDE - 60758-063-05 - (levobunolol hydrochloride)

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Drug Information of LEVOBUNOLOL HYDROCHLORIDE

Product NDC: 60758-063
Proprietary Name: LEVOBUNOLOL HYDROCHLORIDE
Non Proprietary Name: levobunolol hydrochloride
Active Ingredient(s): 2.5    mg/mL & nbsp;   levobunolol hydrochloride
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of LEVOBUNOLOL HYDROCHLORIDE

Product NDC: 60758-063
Labeler Name: Pacific Pharma, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019814
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 19970715

Package Information of LEVOBUNOLOL HYDROCHLORIDE

Package NDC: 60758-063-05
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (60758-063-05) > 5 mL in 1 BOTTLE, DROPPER

NDC Information of LEVOBUNOLOL HYDROCHLORIDE

NDC Code 60758-063-05
Proprietary Name LEVOBUNOLOL HYDROCHLORIDE
Package Description 1 BOTTLE, DROPPER in 1 CARTON (60758-063-05) > 5 mL in 1 BOTTLE, DROPPER
Product NDC 60758-063
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name levobunolol hydrochloride
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 19970715
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Pacific Pharma, Inc.
Substance Name LEVOBUNOLOL HYDROCHLORIDE
Strength Number 2.5
Strength Unit mg/mL
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of LEVOBUNOLOL HYDROCHLORIDE


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