Package 33342-458-07

Brand: nebivolol

Generic: nebivolol
NDC Package

Package Facts

Identity

Package NDC 33342-458-07
Digits Only 3334245807
Product NDC 33342-458
Description

30 TABLET in 1 BOTTLE (33342-458-07)

Marketing

Marketing Status
Marketed Since 2025-01-29
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": "b6c5abdd-bc2d-4ed6-8ca2-8a94c406ed0e", "openfda": {"upc": ["0333342458070", "0333342459077", "0333342460073", "0333342457073"], "unii": ["JGS34J7L9I"], "rxcui": ["387013", "751612", "751618", "827073"], "spl_set_id": ["b6c5abdd-bc2d-4ed6-8ca2-8a94c406ed0e"], "manufacturer_name": ["Macleods Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (33342-458-07)", "package_ndc": "33342-458-07", "marketing_start_date": "20250129"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (33342-458-10)", "package_ndc": "33342-458-10", "marketing_start_date": "20250129"}, {"sample": false, "description": "12 BLISTER PACK in 1 CARTON (33342-458-25)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "33342-458-25", "marketing_start_date": "20250129"}], "brand_name": "Nebivolol", "product_id": "33342-458_b6c5abdd-bc2d-4ed6-8ca2-8a94c406ed0e", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "33342-458", "generic_name": "Nebivolol", "labeler_name": "Macleods Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nebivolol", "active_ingredients": [{"name": "NEBIVOLOL HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA212661", "marketing_category": "ANDA", "marketing_start_date": "20190119", "listing_expiration_date": "20261231"}