Package 72162-2177-1

Brand: bisoprolol

Generic: bisoprolol fumarate
NDC Package

Package Facts

Identity

Package NDC 72162-2177-1
Digits Only 7216221771
Product NDC 72162-2177
Description

100 TABLET, FILM COATED in 1 BOTTLE (72162-2177-1)

Marketing

Marketing Status
Marketed Since 2023-12-07
Brand bisoprolol
Generic bisoprolol fumarate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "134a42de-4b00-48ab-bd5e-8061b1ee3ff5", "openfda": {"unii": ["UR59KN573L"], "rxcui": ["854905"], "spl_set_id": ["78056d0b-2265-4da3-a4fe-b96d98289848"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (72162-2177-1)", "package_ndc": "72162-2177-1", "marketing_start_date": "20231207"}], "brand_name": "Bisoprolol", "product_id": "72162-2177_134a42de-4b00-48ab-bd5e-8061b1ee3ff5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "72162-2177", "generic_name": "Bisoprolol fumarate", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bisoprolol", "active_ingredients": [{"name": "BISOPROLOL FUMARATE", "strength": "5 mg/1"}], "application_number": "ANDA075474", "marketing_category": "ANDA", "marketing_start_date": "20190620", "listing_expiration_date": "20261231"}