Package 50090-5761-2

Brand: nebivolol

Generic: nebivolol
NDC Package

Package Facts

Identity

Package NDC 50090-5761-2
Digits Only 5009057612
Product NDC 50090-5761
Description

90 TABLET in 1 BOTTLE (50090-5761-2)

Marketing

Marketing Status
Marketed Since 2021-10-07
Brand nebivolol
Generic nebivolol
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "26df2438-2d17-4683-b43d-68e6605495b3", "openfda": {"unii": ["JGS34J7L9I"], "rxcui": ["751612"], "spl_set_id": ["cdd7a3c5-d3dd-4a89-97d7-642f96eda21b"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-5761-0)", "package_ndc": "50090-5761-0", "marketing_start_date": "20211001"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-5761-2)", "package_ndc": "50090-5761-2", "marketing_start_date": "20211007"}], "brand_name": "Nebivolol", "product_id": "50090-5761_26df2438-2d17-4683-b43d-68e6605495b3", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "50090-5761", "generic_name": "Nebivolol", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nebivolol", "active_ingredients": [{"name": "NEBIVOLOL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA203828", "marketing_category": "ANDA", "marketing_start_date": "20210916", "listing_expiration_date": "20261231"}