Package 70771-1727-3
Brand: bisoprolol fumarate
Generic: bisoprolol fumaratePackage Facts
Identity
Package NDC
70771-1727-3
Digits Only
7077117273
Product NDC
70771-1727
Description
30 TABLET, FILM COATED in 1 BOTTLE (70771-1727-3)
Marketing
Marketing Status
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": "bd36cf67-11ab-4a1f-b1b6-9d5c078a9206", "openfda": {"unii": ["UR59KN573L"], "rxcui": ["854901", "854905"], "spl_set_id": ["2d380e61-052c-4c33-8a35-01c9eb651d68"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (70771-1727-1)", "package_ndc": "70771-1727-1", "marketing_start_date": "20220915"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (70771-1727-3)", "package_ndc": "70771-1727-3", "marketing_start_date": "20220915"}], "brand_name": "Bisoprolol Fumarate", "product_id": "70771-1727_bd36cf67-11ab-4a1f-b1b6-9d5c078a9206", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "70771-1727", "generic_name": "Bisoprolol Fumarate", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bisoprolol Fumarate", "active_ingredients": [{"name": "BISOPROLOL FUMARATE", "strength": "10 mg/1"}], "application_number": "ANDA215680", "marketing_category": "ANDA", "marketing_start_date": "20220915", "listing_expiration_date": "20261231"}