Package 70518-3527-0

Brand: nebivolol

Generic: nebivolol
NDC Package

Package Facts

Identity

Package NDC 70518-3527-0
Digits Only 7051835270
Product NDC 70518-3527
Product ID 70518-3527_48be4213-e2e2-10b7-e063-6294a90aee17
Description

90 TABLET in 1 BOTTLE, PLASTIC (70518-3527-0)

Marketing

Marketing Status
Marketed Since 2022-09-20
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": "48be4213-e2e2-10b7-e063-6294a90aee17", "openfda": {"unii": ["JGS34J7L9I"], "rxcui": ["387013"], "spl_set_id": ["3745fc9d-cd3f-4877-bef0-81d9a9a05786"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-3527-0)", "package_ndc": "70518-3527-0", "marketing_start_date": "20220920"}], "brand_name": "Nebivolol", "product_id": "70518-3527_48be4213-e2e2-10b7-e063-6294a90aee17", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "70518-3527", "generic_name": "Nebivolol", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nebivolol", "active_ingredients": [{"name": "NEBIVOLOL HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA203828", "marketing_category": "ANDA", "marketing_start_date": "20220920", "listing_expiration_date": "20271231"}