Package 10702-013-01

Brand: betaxolol hydrochloride

Generic: betaxolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 10702-013-01
Digits Only 1070201301
Product NDC 10702-013
Product ID 10702-013_1757ca78-c783-c977-e063-6294a90a7862
Description

100 TABLET, COATED in 1 BOTTLE (10702-013-01)

Marketing

Marketing Status
Marketed Since 2011-11-02
Brand betaxolol hydrochloride
Generic betaxolol hydrochloride
Sample Package No

Linked Drug Pages (1)

BETAXOLOL HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1757ca78-c783-c977-e063-6294a90a7862", "openfda": {"unii": ["6X97D2XT0O"], "rxcui": ["1297753", "1297757"], "spl_set_id": ["f3b50bbb-df03-4ed7-9d8d-180edc2abd54"], "manufacturer_name": ["KVK-TECH, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (10702-013-01)", "package_ndc": "10702-013-01", "marketing_start_date": "20111102"}], "brand_name": "BETAXOLOL HYDROCHLORIDE", "product_id": "10702-013_1757ca78-c783-c977-e063-6294a90a7862", "dosage_form": "TABLET, COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "10702-013", "generic_name": "betaxolol hydrochloride", "labeler_name": "KVK-TECH, INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BETAXOLOL HYDROCHLORIDE", "active_ingredients": [{"name": "BETAXOLOL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA078962", "marketing_category": "ANDA", "marketing_start_date": "20111102", "listing_expiration_date": "20261231"}