Package 42291-873-90

Brand: nebivolol

Generic: nebivolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 42291-873-90
Digits Only 4229187390
Product NDC 42291-873
Description

90 TABLET in 1 BOTTLE (42291-873-90)

Marketing

Marketing Status
Marketed Since 2024-07-10
Brand nebivolol
Generic nebivolol hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "48842030-a03d-fb38-e063-6294a90a9dd0", "openfda": {"upc": ["0342291872905", "0342291874909", "0342291873902"], "unii": ["JGS34J7L9I"], "rxcui": ["387013", "751612", "751618", "827073"], "spl_set_id": ["1ce89dc5-018d-db40-e063-6294a90a9722"], "manufacturer_name": ["AvKARE"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (42291-873-90)", "package_ndc": "42291-873-90", "marketing_start_date": "20240710"}], "brand_name": "nebivolol", "product_id": "42291-873_48842030-a03d-fb38-e063-6294a90a9dd0", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "42291-873", "generic_name": "nebivolol hydrochloride", "labeler_name": "AvKARE", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "nebivolol", "active_ingredients": [{"name": "NEBIVOLOL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA203821", "marketing_category": "ANDA", "marketing_start_date": "20240710", "listing_expiration_date": "20271231"}