Package 65862-086-01

Brand: bisoprolol fumarate

Generic: bisoprolol fumarate
NDC Package

Package Facts

Identity

Package NDC 65862-086-01
Digits Only 6586208601
Product NDC 65862-086
Description

100 TABLET, FILM COATED in 1 BOTTLE (65862-086-01)

Marketing

Marketing Status
Marketed Since 2006-12-27
Brand bisoprolol fumarate
Generic bisoprolol fumarate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "bb3ee6c5-1c46-41c6-890b-d775a103111a", "openfda": {"unii": ["UR59KN573L"], "rxcui": ["854901", "854905"], "spl_set_id": ["2564646d-183c-4759-8726-155a4c22aa2b"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (65862-086-01)", "package_ndc": "65862-086-01", "marketing_start_date": "20061227"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (65862-086-30)", "package_ndc": "65862-086-30", "marketing_start_date": "20061227"}], "brand_name": "Bisoprolol Fumarate", "product_id": "65862-086_bb3ee6c5-1c46-41c6-890b-d775a103111a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "65862-086", "generic_name": "Bisoprolol Fumarate", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bisoprolol Fumarate", "active_ingredients": [{"name": "BISOPROLOL FUMARATE", "strength": "5 mg/1"}], "application_number": "ANDA077910", "marketing_category": "ANDA", "marketing_start_date": "20061227", "listing_expiration_date": "20261231"}