Package 59651-251-01

Brand: nadolol

Generic: nadolol
NDC Package

Package Facts

Identity

Package NDC 59651-251-01
Digits Only 5965125101
Product NDC 59651-251
Description

100 TABLET in 1 BOTTLE (59651-251-01)

Marketing

Marketing Status
Marketed Since 2021-10-29
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": "bfed393e-1baf-439a-8073-998c1a97b276", "openfda": {"nui": ["N0000000161", "N0000175556"], "unii": ["FEN504330V"], "rxcui": ["198006", "198007", "198008"], "spl_set_id": ["44c5352d-89f8-4bd3-9479-1069304562ca"], "pharm_class_epc": ["beta-Adrenergic Blocker [EPC]"], "pharm_class_moa": ["Adrenergic beta-Antagonists [MoA]"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (59651-251-01)", "package_ndc": "59651-251-01", "marketing_start_date": "20211029"}], "brand_name": "Nadolol", "product_id": "59651-251_bfed393e-1baf-439a-8073-998c1a97b276", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "59651-251", "generic_name": "Nadolol", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nadolol", "active_ingredients": [{"name": "NADOLOL", "strength": "40 mg/1"}], "application_number": "ANDA201893", "marketing_category": "ANDA", "marketing_start_date": "20211029", "listing_expiration_date": "20261231"}