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Betaxolol Hydrochloride - 61314-245-02 - (Betaxolol Hydrochloride)

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Drug Information of Betaxolol Hydrochloride

Product NDC: 61314-245
Proprietary Name: Betaxolol Hydrochloride
Non Proprietary Name: Betaxolol Hydrochloride
Active Ingredient(s): 5.6    mg/mL & nbsp;   Betaxolol Hydrochloride
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of Betaxolol Hydrochloride

Product NDC: 61314-245
Labeler Name: Falcon Pharmaceuticals, Ltd.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019270
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20000515

Package Information of Betaxolol Hydrochloride

Package NDC: 61314-245-02
Package Description: 15 mL in 1 BOTTLE, PLASTIC (61314-245-02)

NDC Information of Betaxolol Hydrochloride

NDC Code 61314-245-02
Proprietary Name Betaxolol Hydrochloride
Package Description 15 mL in 1 BOTTLE, PLASTIC (61314-245-02)
Product NDC 61314-245
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Betaxolol Hydrochloride
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 20000515
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Falcon Pharmaceuticals, Ltd.
Substance Name BETAXOLOL HYDROCHLORIDE
Strength Number 5.6
Strength Unit mg/mL
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Betaxolol Hydrochloride


General Information