Package 24658-700-01

Brand: betaxolol

Generic: betaxolol
NDC Package

Package Facts

Identity

Package NDC 24658-700-01
Digits Only 2465870001
Product NDC 24658-700
Product ID 24658-700_7ee988e7-153d-4d55-b4ec-1a8da8f78f1d
Description

100 TABLET, FILM COATED in 1 BOTTLE (24658-700-01)

Marketing

Marketing Status
Marketed Since 2016-12-15
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": "7ee988e7-153d-4d55-b4ec-1a8da8f78f1d", "openfda": {"upc": ["0324658701011"], "unii": ["6X97D2XT0O"], "rxcui": ["1297753", "1297757"], "spl_set_id": ["e198244d-fda3-4015-8c01-390f3f88e238"], "manufacturer_name": ["PuraCap Laboratories LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (24658-700-01)", "package_ndc": "24658-700-01", "marketing_start_date": "20161215"}], "brand_name": "Betaxolol", "product_id": "24658-700_7ee988e7-153d-4d55-b4ec-1a8da8f78f1d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "24658-700", "generic_name": "Betaxolol", "labeler_name": "PuraCap Laboratories 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": "20160822", "listing_expiration_date": "20261231"}