Package 50090-7853-1

Brand: nebivolol

Generic: nebivolol
NDC Package

Package Facts

Identity

Package NDC 50090-7853-1
Digits Only 5009078531
Product NDC 50090-7853
Product ID 50090-7853_caccc638-504d-4309-a952-dda8de1f85c1
Description

30 TABLET in 1 BOTTLE (50090-7853-1)

Marketing

Marketing Status
Marketed Since 2026-01-08
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": "caccc638-504d-4309-a952-dda8de1f85c1", "openfda": {"unii": ["JGS34J7L9I"], "rxcui": ["827073"], "spl_set_id": ["78c20341-4fbf-4c78-9817-03e7e0072f82"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-7853-1)", "package_ndc": "50090-7853-1", "marketing_start_date": "20260108"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7853-2)", "package_ndc": "50090-7853-2", "marketing_start_date": "20260108"}], "brand_name": "NEBIVOLOL", "product_id": "50090-7853_caccc638-504d-4309-a952-dda8de1f85c1", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "50090-7853", "generic_name": "NEBIVOLOL", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NEBIVOLOL", "active_ingredients": [{"name": "NEBIVOLOL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA217397", "marketing_category": "ANDA", "marketing_start_date": "20241001", "listing_expiration_date": "20271231"}