Package 70518-4032-0

Brand: nebivolol

Generic: nebivolol
NDC Package

Package Facts

Identity

Package NDC 70518-4032-0
Digits Only 7051840320
Product NDC 70518-4032
Product ID 70518-4032_3f91fb6d-6d25-a881-e063-6394a90a3c61
Description

90 TABLET in 1 BOTTLE, PLASTIC (70518-4032-0)

Marketing

Marketing Status
Marketed Since 2024-03-05
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": "3f91fb6d-6d25-a881-e063-6394a90a3c61", "openfda": {"nui": ["N0000000161", "N0000175556"], "unii": ["030Y90569U"], "rxcui": ["387013"], "spl_set_id": ["a9bad35e-cd48-48f1-93ca-46490dbf70a8"], "pharm_class_epc": ["beta-Adrenergic Blocker [EPC]"], "pharm_class_moa": ["Adrenergic beta-Antagonists [MoA]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-4032-0)", "package_ndc": "70518-4032-0", "marketing_start_date": "20240305"}], "brand_name": "NEBIVOLOL", "product_id": "70518-4032_3f91fb6d-6d25-a881-e063-6394a90a3c61", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "70518-4032", "generic_name": "nebivolol", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NEBIVOLOL", "active_ingredients": [{"name": "NEBIVOLOL", "strength": "5 mg/1"}], "application_number": "ANDA212682", "marketing_category": "ANDA", "marketing_start_date": "20240305", "listing_expiration_date": "20261231"}