Package 68788-8671-1

Brand: bisoprolol fumarate

Generic: bisoprolol fumarate
NDC Package

Package Facts

Identity

Package NDC 68788-8671-1
Digits Only 6878886711
Product NDC 68788-8671
Description

100 TABLET in 1 BOTTLE, PLASTIC (68788-8671-1)

Marketing

Marketing Status
Marketed Since 2024-05-21
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": "2eb410f7-87a6-4402-9bce-925be3d3c946", "openfda": {"unii": ["UR59KN573L"], "rxcui": ["854905"], "spl_set_id": ["c0e309f3-82c3-4629-b790-fb8538b87369"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (68788-8671-1)", "package_ndc": "68788-8671-1", "marketing_start_date": "20240521"}], "brand_name": "Bisoprolol Fumarate", "product_id": "68788-8671_2eb410f7-87a6-4402-9bce-925be3d3c946", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "68788-8671", "generic_name": "Bisoprolol fumarate", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bisoprolol Fumarate", "active_ingredients": [{"name": "BISOPROLOL FUMARATE", "strength": "5 mg/1"}], "application_number": "ANDA078635", "marketing_category": "ANDA", "marketing_start_date": "20240521", "listing_expiration_date": "20261231"}