Package 63629-9423-1

Brand: nebivolol

Generic: nebivolol
NDC Package

Package Facts

Identity

Package NDC 63629-9423-1
Digits Only 6362994231
Product NDC 63629-9423
Product ID 63629-9423_c8f3a9c6-80ab-4f14-8d59-e9f9bce81663
Description

30 TABLET in 1 BOTTLE (63629-9423-1)

Marketing

Marketing Status
Marketed Since 2022-08-16
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": "c8f3a9c6-80ab-4f14-8d59-e9f9bce81663", "openfda": {"unii": ["JGS34J7L9I"], "rxcui": ["827073"], "spl_set_id": ["0d4b1e1a-d5c3-4bdc-860d-387e8fd0b389"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (63629-9423-1)", "package_ndc": "63629-9423-1", "marketing_start_date": "20220816"}], "brand_name": "Nebivolol", "product_id": "63629-9423_c8f3a9c6-80ab-4f14-8d59-e9f9bce81663", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "63629-9423", "generic_name": "Nebivolol", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nebivolol", "active_ingredients": [{"name": "NEBIVOLOL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA211053", "marketing_category": "ANDA", "marketing_start_date": "20211217", "listing_expiration_date": "20261231"}