Package 42571-325-11

Brand: ranolazine

Generic: ranolazine
NDC Package

Package Facts

Identity

Package NDC 42571-325-11
Digits Only 4257132511
Product NDC 42571-325
Description

100 BLISTER PACK in 1 CARTON (42571-325-11) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (42571-325-32)

Marketing

Marketing Status
Marketed Since 2020-06-01
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": "d172a3c8-ae0a-9ccb-e053-2a95a90a069e", "openfda": {"nui": ["N0000175427", "N0000190114", "N0000185503", "N0000182137", "N0000187061"], "upc": ["0342571324605", "0342571325602"], "unii": ["A6IEZ5M406"], "rxcui": ["616749", "728231"], "spl_set_id": ["f6facddc-c020-436e-8e68-bf9a4223e7cf"], "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": ["Micro Labs Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (42571-325-11)  / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (42571-325-32)", "package_ndc": "42571-325-11", "marketing_start_date": "20200601"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (42571-325-60)", "package_ndc": "42571-325-60", "marketing_start_date": "20200601"}, {"sample": false, "description": "180 TABLET, EXTENDED RELEASE in 1 BOTTLE (42571-325-64)", "package_ndc": "42571-325-64", "marketing_start_date": "20200601"}], "brand_name": "Ranolazine", "product_id": "42571-325_d172a3c8-ae0a-9ccb-e053-2a95a90a069e", "dosage_form": "TABLET, 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": "42571-325", "generic_name": "Ranolazine", "labeler_name": "Micro Labs Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ranolazine", "active_ingredients": [{"name": "RANOLAZINE", "strength": "1000 mg/1"}], "application_number": "ANDA211745", "marketing_category": "ANDA", "marketing_start_date": "20200601", "listing_expiration_date": "20261231"}