Package 59651-009-99

Brand: ranolazine

Generic: ranolazine
NDC Package

Package Facts

Identity

Package NDC 59651-009-99
Digits Only 5965100999
Product NDC 59651-009
Description

1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59651-009-99)

Marketing

Marketing Status
Marketed Since 2022-12-23
Brand ranolazine
Generic ranolazine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ee3c2383-a36a-4abe-9764-89f817798f28", "openfda": {"nui": ["N0000175427", "N0000190114", "N0000185503", "N0000182137", "N0000187061"], "upc": ["0359651009604"], "unii": ["A6IEZ5M406"], "rxcui": ["616749", "728231"], "spl_set_id": ["49873158-5c0a-41da-86a2-369ef6b0cbc8"], "pharm_class_epc": ["Anti-anginal [EPC]"], "pharm_class_moa": ["Cytochrome P450 3A Inhibitors [MoA]", "P-Glycoprotein Inhibitors [MoA]", "Cytochrome P450 2D6 Inhibitors [MoA]", "Organic Cation Transporter 2 Inhibitors [MoA]"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59651-009-18)", "package_ndc": "59651-009-18", "marketing_start_date": "20221223"}, {"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59651-009-60)", "package_ndc": "59651-009-60", "marketing_start_date": "20221223"}, {"sample": false, "description": "1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59651-009-99)", "package_ndc": "59651-009-99", "marketing_start_date": "20221223"}], "brand_name": "Ranolazine", "product_id": "59651-009_ee3c2383-a36a-4abe-9764-89f817798f28", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Anti-anginal [EPC]", "Cytochrome P450 2D6 Inhibitors [MoA]", "Cytochrome P450 3A Inhibitors [MoA]", "Organic Cation Transporter 2 Inhibitors [MoA]", "P-Glycoprotein Inhibitors [MoA]"], "product_ndc": "59651-009", "generic_name": "Ranolazine", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ranolazine", "active_ingredients": [{"name": "RANOLAZINE", "strength": "500 mg/1"}], "application_number": "ANDA209081", "marketing_category": "ANDA", "marketing_start_date": "20221223", "listing_expiration_date": "20261231"}