Package 72162-2417-3

Brand: nebivolol

Generic: nebivolol
NDC Package

Package Facts

Identity

Package NDC 72162-2417-3
Digits Only 7216224173
Product NDC 72162-2417
Product ID 72162-2417_754148cb-fd38-42b8-9434-05a45c1bd89b
Description

30 TABLET in 1 BOTTLE (72162-2417-3)

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": "754148cb-fd38-42b8-9434-05a45c1bd89b", "openfda": {"unii": ["JGS34J7L9I"], "rxcui": ["387013"], "spl_set_id": ["9a5e1bd8-f2b6-42e6-972d-09418528cd63"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72162-2417-3)", "package_ndc": "72162-2417-3", "marketing_start_date": "20241031"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72162-2417-9)", "package_ndc": "72162-2417-9", "marketing_start_date": "20241031"}], "brand_name": "Nebivolol", "product_id": "72162-2417_754148cb-fd38-42b8-9434-05a45c1bd89b", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "72162-2417", "generic_name": "Nebivolol", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nebivolol", "active_ingredients": [{"name": "NEBIVOLOL HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA208717", "marketing_category": "ANDA", "marketing_start_date": "20171229", "listing_expiration_date": "20261231"}