Package 24689-159-02

Brand: nebivolol

Generic: nebivolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 24689-159-02
Digits Only 2468915902
Product NDC 24689-159
Description

90 TABLET in 1 BOTTLE (24689-159-02)

Marketing

Marketing Status
Marketed Since 2024-05-13
Brand nebivolol
Generic nebivolol hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ffc06b5e-4f7d-4020-8be9-a4e903c1bfa8", "openfda": {"unii": ["JGS34J7L9I"], "rxcui": ["387013", "751612", "751618", "827073"], "spl_set_id": ["3f5766c0-e1fa-4805-a32c-523182310ad5"], "manufacturer_name": ["Apnar Pharma LP"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (24689-159-01)", "package_ndc": "24689-159-01", "marketing_start_date": "20240513"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (24689-159-02)", "package_ndc": "24689-159-02", "marketing_start_date": "20240513"}], "brand_name": "nebivolol", "product_id": "24689-159_ffc06b5e-4f7d-4020-8be9-a4e903c1bfa8", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "24689-159", "generic_name": "nebivolol hydrochloride", "labeler_name": "Apnar Pharma LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "nebivolol", "active_ingredients": [{"name": "NEBIVOLOL HYDROCHLORIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA216568", "marketing_category": "ANDA", "marketing_start_date": "20240513", "listing_expiration_date": "20261231"}