Package 72189-592-60

Brand: nebivolol

Generic: nebivolol
NDC Package

Package Facts

Identity

Package NDC 72189-592-60
Digits Only 7218959260
Product NDC 72189-592
Product ID 72189-592_25b5631c-44a4-05b4-e063-6394a90aeb7d
Description

60 TABLET in 1 BOTTLE (72189-592-60)

Marketing

Marketing Status
Marketed Since 2024-10-30
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": "25b5631c-44a4-05b4-e063-6394a90aeb7d", "openfda": {"nui": ["N0000000161", "N0000175556"], "unii": ["030Y90569U"], "rxcui": ["827073"], "spl_set_id": ["25b5631c-44a3-05b4-e063-6394a90aeb7d"], "pharm_class_epc": ["beta-Adrenergic Blocker [EPC]"], "pharm_class_moa": ["Adrenergic beta-Antagonists [MoA]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (72189-592-60)", "package_ndc": "72189-592-60", "marketing_start_date": "20241030"}], "brand_name": "Nebivolol", "product_id": "72189-592_25b5631c-44a4-05b4-e063-6394a90aeb7d", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "72189-592", "generic_name": "Nebivolol", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nebivolol", "active_ingredients": [{"name": "NEBIVOLOL", "strength": "20 mg/1"}], "application_number": "ANDA212682", "marketing_category": "ANDA", "marketing_start_date": "20241030", "listing_expiration_date": "20261231"}