Package 29300-297-01

Brand: ranolazine

Generic: ranolazine
NDC Package

Package Facts

Identity

Package NDC 29300-297-01
Digits Only 2930029701
Product NDC 29300-297
Description

100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (29300-297-01)

Marketing

Marketing Status
Marketed Since 2023-07-15
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": "429d55c7-1e90-4345-a6d4-59f689557f40", "openfda": {"nui": ["N0000175427", "N0000190114", "N0000185503", "N0000182137", "N0000187061"], "unii": ["A6IEZ5M406"], "rxcui": ["616749", "728231"], "spl_set_id": ["e2a8c9f9-5f6a-4496-8fd6-2439e564db4f"], "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": ["Unichem Pharmaceuticals (USA), Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (29300-297-01)", "package_ndc": "29300-297-01", "marketing_start_date": "20230715"}, {"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (29300-297-16)", "package_ndc": "29300-297-16", "marketing_start_date": "20230715"}, {"sample": false, "description": "250 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (29300-297-52)", "package_ndc": "29300-297-52", "marketing_start_date": "20230715"}], "brand_name": "Ranolazine", "product_id": "29300-297_429d55c7-1e90-4345-a6d4-59f689557f40", "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": "29300-297", "generic_name": "Ranolazine", "labeler_name": "Unichem Pharmaceuticals (USA), Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ranolazine", "active_ingredients": [{"name": "RANOLAZINE", "strength": "1000 mg/1"}], "application_number": "ANDA213083", "marketing_category": "ANDA", "marketing_start_date": "20230316", "listing_expiration_date": "20261231"}