Package 72162-2233-1

Brand: nadolol

Generic: nadolol
NDC Package

Package Facts

Identity

Package NDC 72162-2233-1
Digits Only 7216222331
Product NDC 72162-2233
Description

100 TABLET in 1 BOTTLE (72162-2233-1)

Marketing

Marketing Status
Marketed Since 2024-01-26
Brand nadolol
Generic nadolol
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b12a1007-6a59-45ef-95a4-47a3ee16bcfd", "openfda": {"nui": ["N0000000161", "N0000175556"], "unii": ["FEN504330V"], "rxcui": ["198007"], "spl_set_id": ["9cf4ca73-2d38-44c2-a522-d44d536b5e55"], "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": "100 TABLET in 1 BOTTLE (72162-2233-1)", "package_ndc": "72162-2233-1", "marketing_start_date": "20240126"}], "brand_name": "Nadolol", "product_id": "72162-2233_b12a1007-6a59-45ef-95a4-47a3ee16bcfd", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "72162-2233", "generic_name": "Nadolol", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nadolol", "active_ingredients": [{"name": "NADOLOL", "strength": "40 mg/1"}], "application_number": "ANDA203455", "marketing_category": "ANDA", "marketing_start_date": "20160223", "listing_expiration_date": "20261231"}