Package 59651-138-90

Brand: nebivolol

Generic: nebivolol
NDC Package

Package Facts

Identity

Package NDC 59651-138-90
Digits Only 5965113890
Product NDC 59651-138
Product ID 59651-138_8b2201ae-7174-45fe-a219-63d385d5c94b
Description

90 TABLET in 1 BOTTLE (59651-138-90)

Marketing

Marketing Status
Marketed Since 2021-12-17
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": "8b2201ae-7174-45fe-a219-63d385d5c94b", "openfda": {"upc": ["0359651137307"], "unii": ["JGS34J7L9I"], "rxcui": ["387013", "751612", "751618", "827073"], "spl_set_id": ["6e43a4e2-574e-4f4a-804d-e346b4edd2f1"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (59651-138-30)", "package_ndc": "59651-138-30", "marketing_start_date": "20211217"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (59651-138-90)", "package_ndc": "59651-138-90", "marketing_start_date": "20211217"}], "brand_name": "Nebivolol", "product_id": "59651-138_8b2201ae-7174-45fe-a219-63d385d5c94b", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "59651-138", "generic_name": "Nebivolol", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nebivolol", "active_ingredients": [{"name": "NEBIVOLOL HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA211053", "marketing_category": "ANDA", "marketing_start_date": "20211217", "listing_expiration_date": "20261231"}