Package 72241-033-04

Brand: nebivolol

Generic: nebivolol
NDC Package

Package Facts

Identity

Package NDC 72241-033-04
Digits Only 7224103304
Product NDC 72241-033
Description

90 TABLET in 1 BOTTLE (72241-033-04)

Marketing

Marketing Status
Marketed Since 2021-12-18
Brand nebivolol
Generic nebivolol
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "53d2f49b-b0b8-46fc-b80d-1ac3756e7e7c", "openfda": {"upc": ["0372241032110", "0372241034053", "0372241034220", "0372241033223", "0372241035227", "0372241033117"], "unii": ["JGS34J7L9I"], "rxcui": ["387013", "751612", "751618", "827073"], "spl_set_id": ["19d20396-ade8-400e-94f4-69913637d051"], "manufacturer_name": ["Modavar Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (72241-033-04)", "package_ndc": "72241-033-04", "marketing_start_date": "20211218"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (72241-033-05)", "package_ndc": "72241-033-05", "marketing_start_date": "20211218"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (72241-033-11)", "package_ndc": "72241-033-11", "marketing_start_date": "20211218"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (72241-033-22)", "package_ndc": "72241-033-22", "marketing_start_date": "20211218"}], "brand_name": "Nebivolol", "product_id": "72241-033_53d2f49b-b0b8-46fc-b80d-1ac3756e7e7c", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "72241-033", "generic_name": "Nebivolol", "labeler_name": "Modavar Pharmaceuticals LLC", "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"}