Package 42806-038-01

Brand: betaxolol

Generic: betaxolol
NDC Package

Package Facts

Identity

Package NDC 42806-038-01
Digits Only 4280603801
Product NDC 42806-038
Product ID 42806-038_666cb1d9-ec1f-453a-be4f-fafa2b67c1fd
Description

100 TABLET, FILM COATED in 1 BOTTLE (42806-038-01)

Marketing

Marketing Status
Marketed Since 2010-07-20
Brand betaxolol
Generic betaxolol
Sample Package No

Linked Drug Pages (1)

Betaxolol ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "666cb1d9-ec1f-453a-be4f-fafa2b67c1fd", "openfda": {"unii": ["6X97D2XT0O"], "rxcui": ["1297753", "1297757"], "spl_set_id": ["bf716efe-0a9f-43b1-9d8a-c69330b82e18"], "manufacturer_name": ["Epic Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (42806-038-01)", "package_ndc": "42806-038-01", "marketing_start_date": "20100720"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (42806-038-10)", "package_ndc": "42806-038-10", "marketing_start_date": "20100720"}], "brand_name": "Betaxolol", "product_id": "42806-038_666cb1d9-ec1f-453a-be4f-fafa2b67c1fd", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "42806-038", "generic_name": "Betaxolol", "labeler_name": "Epic Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Betaxolol", "active_ingredients": [{"name": "BETAXOLOL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA075541", "marketing_category": "ANDA", "marketing_start_date": "20100720", "listing_expiration_date": "20261231"}