Package 72162-2415-3

Brand: nebivolol

Generic: nebivolol
NDC Package

Package Facts

Identity

Package NDC 72162-2415-3
Digits Only 7216224153
Product NDC 72162-2415
Product ID 72162-2415_2124870a-c883-46ee-8f1d-bcb1c01ef301
Description

30 TABLET in 1 BOTTLE (72162-2415-3)

Marketing

Marketing Status
Marketed Since 2024-10-31
Brand nebivolol
Generic nebivolol
Sample Package No

Linked Drug Pages (1)

Nebivolol ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2124870a-c883-46ee-8f1d-bcb1c01ef301", "openfda": {"unii": ["JGS34J7L9I"], "rxcui": ["751618"], "spl_set_id": ["abb0546f-08dd-4354-8b41-d17065b52c24"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72162-2415-3)", "package_ndc": "72162-2415-3", "marketing_start_date": "20241031"}], "brand_name": "Nebivolol", "product_id": "72162-2415_2124870a-c883-46ee-8f1d-bcb1c01ef301", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "72162-2415", "generic_name": "Nebivolol", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nebivolol", "active_ingredients": [{"name": "NEBIVOLOL HYDROCHLORIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA208717", "marketing_category": "ANDA", "marketing_start_date": "20171229", "listing_expiration_date": "20261231"}