Package 71335-2516-1

Brand: nebivolol

Generic: nebivolol
NDC Package

Package Facts

Identity

Package NDC 71335-2516-1
Digits Only 7133525161
Product NDC 71335-2516
Product ID 71335-2516_afe4a662-64fe-49a5-a45c-2bee2070ef85
Description

30 TABLET in 1 BOTTLE (71335-2516-1)

Marketing

Marketing Status
Marketed Since 2024-10-24
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": "afe4a662-64fe-49a5-a45c-2bee2070ef85", "openfda": {"nui": ["N0000000161", "N0000175556"], "unii": ["030Y90569U"], "rxcui": ["387013"], "spl_set_id": ["126de78c-fb3d-4a53-9aaf-f2dfe1ac2a2f"], "pharm_class_epc": ["beta-Adrenergic Blocker [EPC]"], "pharm_class_moa": ["Adrenergic beta-Antagonists [MoA]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-2516-1)", "package_ndc": "71335-2516-1", "marketing_start_date": "20241024"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-2516-2)", "package_ndc": "71335-2516-2", "marketing_start_date": "20241024"}], "brand_name": "NEBIVOLOL", "product_id": "71335-2516_afe4a662-64fe-49a5-a45c-2bee2070ef85", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "71335-2516", "generic_name": "nebivolol", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NEBIVOLOL", "active_ingredients": [{"name": "NEBIVOLOL", "strength": "5 mg/1"}], "application_number": "ANDA212682", "marketing_category": "ANDA", "marketing_start_date": "20220214", "listing_expiration_date": "20261231"}