Package 52817-268-30

Brand: bisoprolol fumarate

Generic: bisoprolol fumarate
NDC Package

Package Facts

Identity

Package NDC 52817-268-30
Digits Only 5281726830
Product NDC 52817-268
Product ID 52817-268_32f899b9-1d84-7c3d-e063-6394a90a502c
Description

30 TABLET, FILM COATED in 1 BOTTLE (52817-268-30)

Marketing

Marketing Status
Marketed Since 2025-03-07
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": "32f899b9-1d84-7c3d-e063-6394a90a502c", "openfda": {"upc": ["0352817268303"], "unii": ["UR59KN573L"], "rxcui": ["865155"], "spl_set_id": ["0ef9e45c-21ee-4e00-a9b8-280e2035b4d3"], "manufacturer_name": ["TruPharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (52817-268-30)", "package_ndc": "52817-268-30", "marketing_start_date": "20250307"}], "brand_name": "Bisoprolol Fumarate", "product_id": "52817-268_32f899b9-1d84-7c3d-e063-6394a90a502c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "52817-268", "generic_name": "Bisoprolol Fumarate", "labeler_name": "TruPharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bisoprolol Fumarate", "active_ingredients": [{"name": "BISOPROLOL FUMARATE", "strength": "2.5 mg/1"}], "application_number": "ANDA075643", "marketing_category": "ANDA", "marketing_start_date": "20250307", "listing_expiration_date": "20261231"}