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Levobunolol Hydrochloride - 61314-229-10 - (Levobunolol Hydrochloride)

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Drug Information of Levobunolol Hydrochloride

Product NDC: 61314-229
Proprietary Name: Levobunolol Hydrochloride
Non Proprietary Name: Levobunolol Hydrochloride
Active Ingredient(s): 5    mg/mL & nbsp;   Levobunolol Hydrochloride
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Levobunolol Hydrochloride

Product NDC: 61314-229
Labeler Name: Falcon Pharmaceuticals, Ltd.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074850
Marketing Category: ANDA
Start Marketing Date: 19970130

Package Information of Levobunolol Hydrochloride

Package NDC: 61314-229-10
Package Description: 10 mL in 1 BOTTLE, PLASTIC (61314-229-10)

NDC Information of Levobunolol Hydrochloride

NDC Code 61314-229-10
Proprietary Name Levobunolol Hydrochloride
Package Description 10 mL in 1 BOTTLE, PLASTIC (61314-229-10)
Product NDC 61314-229
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levobunolol Hydrochloride
Dosage Form Name SOLUTION
Route Name OPHTHALMIC
Start Marketing Date 19970130
Marketing Category Name ANDA
Labeler Name Falcon Pharmaceuticals, Ltd.
Substance Name LEVOBUNOLOL HYDROCHLORIDE
Strength Number 5
Strength Unit mg/mL
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Levobunolol Hydrochloride


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