Betaxolol - 60429-754-01 - (Betaxolol)

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Drug Information of Betaxolol

Product NDC: 60429-754
Proprietary Name: Betaxolol
Non Proprietary Name: Betaxolol
Active Ingredient(s): 20    mg/1 & nbsp;   Betaxolol
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Betaxolol

Product NDC: 60429-754
Labeler Name: Golden State Medical Supply, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078962
Marketing Category: ANDA
Start Marketing Date: 20080627

Package Information of Betaxolol

Package NDC: 60429-754-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (60429-754-01)

NDC Information of Betaxolol

NDC Code 60429-754-01
Proprietary Name Betaxolol
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (60429-754-01)
Product NDC 60429-754
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Betaxolol
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20080627
Marketing Category Name ANDA
Labeler Name Golden State Medical Supply, Inc.
Substance Name BETAXOLOL HYDROCHLORIDE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Betaxolol


General Information