Package 63629-4693-1

Brand: nebivolol

Generic: nebivolol
NDC Package

Package Facts

Identity

Package NDC 63629-4693-1
Digits Only 6362946931
Product NDC 63629-4693
Product ID 63629-4693_31377ec0-88f3-4d00-8cfc-8a4c63750e7f
Description

30 TABLET in 1 BOTTLE (63629-4693-1)

Marketing

Marketing Status
Marketed Since 2024-10-22
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": "31377ec0-88f3-4d00-8cfc-8a4c63750e7f", "openfda": {"unii": ["JGS34J7L9I"], "rxcui": ["387013"], "spl_set_id": ["90d4ea48-7831-4cb0-8796-1ed79407c363"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (63629-4693-1)", "package_ndc": "63629-4693-1", "marketing_start_date": "20241022"}], "brand_name": "Nebivolol", "product_id": "63629-4693_31377ec0-88f3-4d00-8cfc-8a4c63750e7f", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "63629-4693", "generic_name": "Nebivolol", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nebivolol", "active_ingredients": [{"name": "NEBIVOLOL HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA203825", "marketing_category": "ANDA", "marketing_start_date": "20210917", "listing_expiration_date": "20261231"}