Package 71335-2648-2

Brand: nebivolol

Generic: nebivolol
NDC Package

Package Facts

Identity

Package NDC 71335-2648-2
Digits Only 7133526482
Product NDC 71335-2648
Product ID 71335-2648_366e45a3-20d8-4707-ba64-d12985872b58
Description

90 TABLET in 1 BOTTLE (71335-2648-2)

Marketing

Marketing Status
Marketed Since 2025-06-03
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": "366e45a3-20d8-4707-ba64-d12985872b58", "openfda": {"unii": ["JGS34J7L9I"], "rxcui": ["387013"], "spl_set_id": ["156c41be-551b-46ab-86a8-52f6f70a4689"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-2648-1)", "package_ndc": "71335-2648-1", "marketing_start_date": "20250603"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-2648-2)", "package_ndc": "71335-2648-2", "marketing_start_date": "20250603"}], "brand_name": "NEBIVOLOL", "product_id": "71335-2648_366e45a3-20d8-4707-ba64-d12985872b58", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "71335-2648", "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": "ANDA217397", "marketing_category": "ANDA", "marketing_start_date": "20241001", "listing_expiration_date": "20261231"}