Package 0456-1402-90
Brand: bystolic
Generic: nebivolol hydrochloridePackage Facts
Identity
Package NDC
0456-1402-90
Digits Only
0456140290
Product NDC
0456-1402
Description
90 TABLET in 1 BOTTLE (0456-1402-90)
Marketing
Marketing Status
Brand
bystolic
Generic
nebivolol hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0096cdf0-43e6-4128-8990-aed7e1fab83f", "openfda": {"upc": ["0304561405909", "0304561402304", "0304561420902", "0304561410903"], "unii": ["JGS34J7L9I"], "rxcui": ["387013", "751612", "751616", "751618", "751620", "751623", "827073", "827075"], "spl_set_id": ["8b8ad213-1dc8-454e-a524-075685c0e1a8"], "manufacturer_name": ["Allergan, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0456-1402-01)", "package_ndc": "0456-1402-01", "marketing_start_date": "20080122"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (0456-1402-30)", "package_ndc": "0456-1402-30", "marketing_start_date": "20080122"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (0456-1402-90)", "package_ndc": "0456-1402-90", "marketing_start_date": "20080122"}], "brand_name": "Bystolic", "product_id": "0456-1402_0096cdf0-43e6-4128-8990-aed7e1fab83f", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "0456-1402", "generic_name": "nebivolol hydrochloride", "labeler_name": "Allergan, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bystolic", "active_ingredients": [{"name": "NEBIVOLOL HYDROCHLORIDE", "strength": "2.5 mg/1"}], "application_number": "NDA021742", "marketing_category": "NDA", "marketing_start_date": "20080122", "listing_expiration_date": "20261231"}