Betaxolol Hydrochloride 10702-0014-01

Package NDC

10702-0014-01

Manufacturer: Kvk-Tech, Inc.
Dosage Form: Tablet, Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: November 2, 2011
Listing Expires: December 31, 2026
Application: ANDA078962

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Active Ingredients

Ingredient	Strength
Betaxolol Hydrochloride	20 mg/1

Drug Class

Adrenergic beta-Antagonists [MoA]beta-Adrenergic Blocker [EPC]

Selected Package

10702-0014-01Selected

100 TABLET, COATED in 1 BOTTLE (10702-014-01)