Package 72789-395-82

Brand: bisoprolol fumarate

Generic: bisoprolol fumarate
NDC Package

Package Facts

Identity

Package NDC 72789-395-82
Digits Only 7278939582
Product NDC 72789-395
Product ID 72789-395_31f67825-d007-651f-e063-6394a90abab8
Description

500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-395-82)

Marketing

Marketing Status
Marketed Since 2024-03-10
Brand bisoprolol fumarate
Generic bisoprolol fumarate
Sample Package No

Linked Drug Pages (1)

BISOPROLOL FUMARATE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "31f67825-d007-651f-e063-6394a90abab8", "openfda": {"upc": ["0372789395821"], "unii": ["UR59KN573L"], "rxcui": ["854901"], "spl_set_id": ["6566dcbe-3e25-4828-9c10-3d041000bc77"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-395-82)", "package_ndc": "72789-395-82", "marketing_start_date": "20240310"}], "brand_name": "BISOPROLOL FUMARATE", "product_id": "72789-395_31f67825-d007-651f-e063-6394a90abab8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "72789-395", "generic_name": "BISOPROLOL FUMARATE", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BISOPROLOL FUMARATE", "active_ingredients": [{"name": "BISOPROLOL FUMARATE", "strength": "10 mg/1"}], "application_number": "ANDA217617", "marketing_category": "ANDA", "marketing_start_date": "20240310", "listing_expiration_date": "20261231"}