Package 60687-679-21

Brand: bisoprolol fumarate

Generic: bisoprolol fumarate
NDC Package

Package Facts

Identity

Package NDC 60687-679-21
Digits Only 6068767921
Product NDC 60687-679
Description

30 BLISTER PACK in 1 CARTON (60687-679-21) / 1 TABLET in 1 BLISTER PACK (60687-679-11)

Marketing

Marketing Status
Marketed Since 2023-04-20
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": "253e530d-88da-d032-e063-6394a90a7641", "openfda": {"unii": ["UR59KN573L"], "rxcui": ["854905"], "spl_set_id": ["36b53e7f-e306-40a8-8d1b-d00695a4fe61"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (60687-679-21)  / 1 TABLET in 1 BLISTER PACK (60687-679-11)", "package_ndc": "60687-679-21", "marketing_start_date": "20230420"}], "brand_name": "Bisoprolol Fumarate", "product_id": "60687-679_253e530d-88da-d032-e063-6394a90a7641", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "60687-679", "generic_name": "Bisoprolol fumarate", "labeler_name": "American Health Packaging", "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": "20230420", "listing_expiration_date": "20261231"}