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Levobunolol Hydrochloride - 24208-545-10 - (Levobunolol Hydrochloride)

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Drug Information of Levobunolol Hydrochloride

Product NDC: 24208-545
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: 24208-545
Labeler Name: Bausch & Lomb Incorporated
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074307
Marketing Category: ANDA
Start Marketing Date: 19940304

Package Information of Levobunolol Hydrochloride

Package NDC: 24208-545-10
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (24208-545-10) > 10 mL in 1 BOTTLE, DROPPER

NDC Information of Levobunolol Hydrochloride

NDC Code 24208-545-10
Proprietary Name Levobunolol Hydrochloride
Package Description 1 BOTTLE, DROPPER in 1 CARTON (24208-545-10) > 10 mL in 1 BOTTLE, DROPPER
Product NDC 24208-545
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levobunolol Hydrochloride
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 19940304
Marketing Category Name ANDA
Labeler Name Bausch & Lomb Incorporated
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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