Package 16714-529-02

Brand: bisoprolol fumarate

Generic: bisoprolol fumarate
NDC Package

Package Facts

Identity

Package NDC 16714-529-02
Digits Only 1671452902
Product NDC 16714-529
Product ID 16714-529_169e7bf6-19d7-4dc5-bfc7-35c5a8e4cf18
Description

100 TABLET, FILM COATED in 1 BOTTLE (16714-529-02)

Marketing

Marketing Status
Marketed Since 2006-12-27
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": "169e7bf6-19d7-4dc5-bfc7-35c5a8e4cf18", "openfda": {"unii": ["UR59KN573L"], "rxcui": ["854901", "854905"], "spl_set_id": ["4bf3278c-116f-4db7-9af0-08faaf7691a4"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (16714-529-01)", "package_ndc": "16714-529-01", "marketing_start_date": "20061227"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (16714-529-02)", "package_ndc": "16714-529-02", "marketing_start_date": "20061227"}], "brand_name": "Bisoprolol Fumarate", "product_id": "16714-529_169e7bf6-19d7-4dc5-bfc7-35c5a8e4cf18", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "16714-529", "generic_name": "Bisoprolol Fumarate", "labeler_name": "NorthStar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bisoprolol Fumarate", "active_ingredients": [{"name": "BISOPROLOL FUMARATE", "strength": "5 mg/1"}], "application_number": "ANDA077910", "marketing_category": "ANDA", "marketing_start_date": "20061227", "listing_expiration_date": "20261231"}