Betaxolol - 17478-705-25 - (Betaxolol Hydrochloride)

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Drug Information of Betaxolol

Product NDC: 17478-705
Proprietary Name: Betaxolol
Non Proprietary Name: Betaxolol Hydrochloride
Active Ingredient(s): 5    mg/mL & nbsp;   Betaxolol Hydrochloride
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of Betaxolol

Product NDC: 17478-705
Labeler Name: Akorn, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075386
Marketing Category: ANDA
Start Marketing Date: 20030401

Package Information of Betaxolol

Package NDC: 17478-705-25
Package Description: 1 VIAL in 1 CARTON (17478-705-25) > 2.5 mL in 1 VIAL

NDC Information of Betaxolol

NDC Code 17478-705-25
Proprietary Name Betaxolol
Package Description 1 VIAL in 1 CARTON (17478-705-25) > 2.5 mL in 1 VIAL
Product NDC 17478-705
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Betaxolol Hydrochloride
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 20030401
Marketing Category Name ANDA
Labeler Name Akorn, Inc.
Substance Name BETAXOLOL HYDROCHLORIDE
Strength Number 5
Strength Unit mg/mL
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Betaxolol


General Information